Is Sandoz Industrial Products S.A FDA approved?

Sandoz Industrial Products S.A holds 5 FDA-registered establishments across 3 countries. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.

Where are Sandoz Industrial Products S.A's drugs manufactured?

At registered sites in Austria, Spain, India. The FDA register lists Kundl; Langkampfen; Palafolls; Navi Mumbai. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, relabelling, repackaging.

What drugs does Sandoz Industrial Products S.A make?

441 products are listed under Sandoz Industrial Products S.A in the openFDA NDC Directory, most often as injection, solution; tablet, film coated; injection. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Are any Sandoz Industrial Products S.A products in shortage?

11 presentations are currently listed in the FDA drug shortage database under Sandoz Industrial Products S.A, covering Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet, Clindamycin Phosphate Injection, Rocuronium Bromide Injection.

Sandoz Industrial Products S.A

Data as of 28 Sept 2026 · How to read this entry

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Registered sites: 5
Active NDC listings: 438
Labeller names: 5
Live patents: 9
Shortage listings: 38
Countries: 3
Base: Austria

Authorisation

Registered operations

Analytical testing5Active ingredient (API) manufacture3Labelling2Finished drug manufacture5Packaging4Relabelling2Repackaging4

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Sandoz GmbH	Biochemiestrasse 10, Kundl, Tyrol A-6250, Austria (AUT)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging	3002806523300220969
Sandoz GmbH	Biochemiestrasse 10, Langkampfen, Tyrol A-6336, Austria (AUT)	Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging, Relabelling, Repackaging	3004828473301698247
Sandoz Industrial Products S.A	CALLE GORG MOLI D'EN PUIGVERD, 37 - 41, PG MAS PUIGVERD, Palafolls, Barc 08389, Spain (ESP)	Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture	3005403245460091325
SANDOZ PRIVATE LIMITEDRegistrant: Sandoz Private Limited	Plot No.8-A 1/1, TTC Industrial Area, Kalwe Block, Village Dighe, Navi Mumbai, Maharashtra 400708, India (IND)	Analytical testing, Finished drug manufacture, Packaging, Repackaging	3027620173929597674
Sandoz Private Limited	Plot No. 8-A/2 and 8-B, TTC Industrial Area Kalwe Block, Village Dighe, Navi Mumbai, Maharashtra 400708, India (IND)	Analytical testing, Finished drug manufacture, Packaging, Repackaging	3004944629916438583

Alert

Drug shortage listings

Drug	Presentation	Status	Availability	Posted / updated
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatry	Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 5 mg; 5 mg; 5 mg; 5 mg (NDC 0185-0853-01)	Current	Available	12 Oct 202218 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatry	Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 7.5 mg; 7.5 mg; 7.5 mg; 7.5 mg (NDC 0185-2099-01)	Current	Available	12 Oct 202218 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatry	Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 1.25 mg; 1.25 mg; 1.25 mg; 1.25 mg (NDC 0185-2098-01)	Current	Available	12 Oct 202218 Sept 2026
Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate TabletPsychiatry	Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate, Tablet, 2.5 mg; 2.5 mg; 2.5 mg; 2.5 mg (NDC 0185-0842-01)	Current	Available	12 Oct 202218 Sept 2026
Clindamycin Phosphate InjectionAnti-Infective	Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 0781-3289-09)	Current	Available	21 Mar 202318 Sept 2026
Clindamycin Phosphate InjectionAnti-Infective	Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 6 mg/1 mL (NDC 0781-3288-09)	Current	Available	21 Mar 202318 Sept 2026
Clindamycin Phosphate InjectionAnti-Infective	Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 12 mg/1 mL (NDC 72572-074-24)	Current	Available	21 Mar 202318 Sept 2026
Clindamycin Phosphate InjectionAnti-Infective	Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 18 mg/1 mL (NDC 72572-076-24)	Current	Available	21 Mar 202318 Sept 2026
Clindamycin Phosphate InjectionAnti-Infective	Clindamycin Phosphate In 5% Dextrose In Plastic Container, Injection, 18 mg/1 mL (NDC 0781-3290-09)	Current	Available	21 Mar 202318 Sept 2026
Rocuronium Bromide InjectionAnesthesia	Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 0781-3220-92)	Current	Available	15 Feb 202318 Sept 2026
Rocuronium Bromide InjectionAnesthesia	Rocuronium Bromide, Injection, 10 mg/1 mL (NDC 0781-3220-95)	Current	Available	15 Feb 202318 Sept 2026
Fluvastatin Sodium Tablet, Extended ReleaseCardiovascular	Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-01)	To Be Discontinued	-	27 Jan 202627 Jan 2026
Fluvastatin Sodium Tablet, Extended ReleaseCardiovascular	Fluvastatin Sodium, Tablet, Extended Release, 80 mg (NDC 0781-8017-31)	To Be Discontinued	-	27 Jan 202627 Jan 2026
Fluvastatin Sodium Tablet, Extended ReleaseCardiovascular	Lescol XL, Tablet, Extended Release, 80 mg (NDC 66758-211-31)	To Be Discontinued	-	27 Jan 202627 Jan 2026
Adalimumab-adaz InjectionRheumatology	Hyrimoz, Injection, 40 mg/.4 mL (NDC 61314-473-64)	To Be Discontinued	-	13 Jan 202613 Jan 2026
Adalimumab-adaz InjectionRheumatology	Hyrimoz, Injection, 80 mg/.8 mL (NDC 61314-454-68)	To Be Discontinued	-	13 Jan 202613 Jan 2026
Adalimumab-adaz InjectionRheumatology	Hyrimoz, Injection, 80 mg/.8 mL (NDC 61314-454-36)	To Be Discontinued	-	13 Jan 202613 Jan 2026
Adalimumab-adaz InjectionRheumatology	Hyrimoz, Injection, Kit (NDC 61314-531-64)	To Be Discontinued	-	13 Jan 202613 Jan 2026
Adalimumab-adaz InjectionRheumatology	Hyrimoz, Injection, Kit (NDC 61314-517-36)	To Be Discontinued	-	13 Jan 202613 Jan 2026
Ampicillin Sodium InjectionAnti-Infective	Ampicillin Sodium, Injection, 2 g (NDC 0781-9408-95)	To Be Discontinued	-	8 Dec 20258 Dec 2025
Ampicillin Sodium InjectionAnti-Infective	Ampicillin Sodium, Injection, 1 g (NDC 0781-9412-92)	To Be Discontinued	-	8 Dec 20258 Dec 2025
Ampicillin Sodium InjectionAnti-Infective	Ampicillin Sodium, Injection, 1 g (NDC 0781-9404-95)	To Be Discontinued	-	8 Dec 20258 Dec 2025
Ampicillin Sodium InjectionAnti-Infective	Ampicillin Sodium, Injection, 10 g (NDC 0781-9409-95)	To Be Discontinued	-	8 Dec 20258 Dec 2025
Ampicillin Sodium InjectionAnti-Infective	Ampicillin Sodium, Injection, 2 g (NDC 0781-9413-92)	To Be Discontinued	-	8 Dec 20258 Dec 2025
Oxaliplatin InjectionOncology	Oxaliplatin, Injection, 5 mg/1 mL (NDC 0781-3315-70)	To Be Discontinued	-	20 Oct 202520 Oct 2025
Oxaliplatin InjectionOncology	Oxaliplatin, Injection, 5 mg/1 mL (NDC 0781-3317-80)	To Be Discontinued	-	20 Oct 202520 Oct 2025
Pemetrexed Disodium InjectionOncology	Pemetrexed Disodium, Injection, 100 mg/4 mL (NDC 0781-3518-76)	To Be Discontinued	-	10 Oct 202510 Oct 2025
Pemetrexed Disodium InjectionOncology	Pemetrexed Disodium, Injection, 500 mg/20 mL (NDC 0781-3519-90)	To Be Discontinued	-	10 Oct 202510 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 20 mg (NDC 0781-2868-01)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 20 mg (NDC 0781-2868-10)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 20 mg (NDC 0781-2868-31)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 40 mg (NDC 0781-2234-01)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 20 mg (NDC 0781-2868-92)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 40 mg (NDC 0781-2234-10)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 10 mg (NDC 0781-2859-01)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 10 mg (NDC 0781-2859-10)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 10 mg (NDC 0781-2859-31)	To Be Discontinued	-	9 Oct 20259 Oct 2025
Omeprazole Delayed Release CapsuleGastroenterology	Omeprazole, Delayed Release Capsule, 40 mg (NDC 0781-2234-31)	To Be Discontinued	-	9 Oct 20259 Oct 2025

Catalogue

Drug listings by form and route

438

438 active NDC listings: 426 human prescription drug, 8 bulk ingredient, 3 human otc drug, 1 drug for further processing. By marketing category: ANDA 288, NDA AUTHORIZED GENERIC 64, NDA 53, BLA 24, BULK INGREDIENT 8.

Dosage form	NDCs
injection, solution	56
tablet, film coated	52
injection	48
tablet	38
injection, powder, for solution	37
capsule	33
capsule, extended release	28
solution/ drops	18
patch, extended release	16
solution	16
kit	14
injection, powder, lyophilized, for solution	12
powder	9
suspension/ drops	8
patch	6

Route	NDCs
oral	182
intravenous	122
ophthalmic	46
subcutaneous	45
intramuscular	35
transdermal	22
parenteral	13
auricular (otic)	5
intravitreal	3
respiratory (inhalation)	3
intraocular	1
topical	1

Labeller name on the listing	NDCs
sandoz inc	378
sandoz inc.	46
sandoz gmbh	8
sandoz inc	3
sandoz, inc.	3

Exclusivity

Patents and exclusivities

Patent	Product	Covers	Expiry
8323630	TRAVATAN Ztravoprost	product	Sept 2027
8388941	TRAVATAN Ztravoprost	product	Sept 2027
7932241	RECLASTzoledronic acid	product	Feb 2028
7582727	ANGIOMAXbivalirudin	product	Jul 2028
7598343	ANGIOMAXbivalirudin	product	Jul 2028
7932241*PED	RECLASTzoledronic acid	use	Aug 2028
7582727*PED	ANGIOMAXbivalirudin	use	Jan 2029
7598343*PED	ANGIOMAXbivalirudin	use	Jan 2029
8268299	TRAVATAN Ztravoprost	product	Oct 2029

Catalogue

Marketed products

441

Showing 150 of 441.

Brand	Generic name	Form / route	NDC
Acetaminophen	acetaminophen	injection, solution, intravenous	0781-3156ANDA
Acetaminophen	acetaminophen	injection, solution, intravenous	0781-9274ANDA
Adalimumab	adalimumab-adaz	injection, solution, subcutaneous	61314-325BLA
Adalimumab	adalimumab-adaz	injection, solution, subcutaneous	61314-327BLA
Adalimumab	adalimumab-adaz	injection, solution, subcutaneous	61314-332BLA
Adalimumab	adalimumab-adaz	injection, solution, subcutaneous	61314-391BLA
Albuterol Sulfate	Albuterol Sulfate	aerosol, metered, respiratory (inhalation)	0781-7296NDA AUTHORIZED GENERIC
Alprazolam	Alprazolam	tablet, oral	0781-1061ANDA
Alprazolam	Alprazolam	tablet, oral	0781-1077ANDA
Alprazolam	Alprazolam	tablet, oral	0781-1079ANDA
Alprazolam	Alprazolam	tablet, oral	0781-1089ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1486ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1487ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1488ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1489ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1490ANDA
Amitriptyline Hydrochloride	Amitriptyline Hydrochloride	tablet, film coated, oral	0781-1491ANDA
Amoxicillin	Amoxicillin	capsule, oral	0781-2020ANDA
Amoxicillin	Amoxicillin	capsule, oral	0781-2613ANDA
Amoxicillin	Amoxicillin	tablet, film coated, oral	0781-5060ANDA
Amoxicillin	Amoxicillin	tablet, film coated, oral	0781-5061ANDA
Amoxicillin	Amoxicillin	powder, for suspension, oral	0781-6039ANDA
Amoxicillin	Amoxicillin	powder, for suspension, oral	0781-6041ANDA
Amoxicillin	Amoxicillin	powder, for suspension, oral	0781-6156ANDA
Amoxicillin	Amoxicillin	powder, for suspension, oral	0781-6157ANDA
-	Amoxicillin Trihydrate	powder	43858-715BULK INGREDIENT
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	tablet, film coated, oral	0781-1831ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	tablet, film coated, oral	0781-1852ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	tablet, film coated, oral	0781-1874ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	tablet, multilayer, extended release, oral	0781-1943ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	powder, for suspension, oral	0781-6102ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	powder, for suspension, oral	0781-6104ANDA
Amoxicillin and Clavulanate Potassium	Amoxicillin and Clavulanate Potassium	suspension, oral	0781-6139ANDA
Ampicillin	Ampicillin	capsule, oral	0781-2145ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-3400ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-3402ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-3404ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-3407ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-3408ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-3409ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-3412ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-3413ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9242ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9250ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9261ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9273ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9401ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9402ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9404ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9407ANDA
Ampicillin	Ampicillin sodium	injection, powder, for solution, intramuscular, intravenous	0781-9408ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-9409ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-9412ANDA
Ampicillin	Ampicillin Sodium	injection, powder, for solution, intravenous	0781-9413ANDA
Anectine	Succinylcholine Chloride	injection, solution, intramuscular, intravenous, parenteral	0781-3411NDA
Anectine	Succinylcholine Chloride	injection, solution, intramuscular, intravenous, parenteral	0781-9053NDA
Apraclonidine	Apraclonidine	solution, ophthalmic	61314-665NDA AUTHORIZED GENERIC
Aprepitant	aprepitant	capsule, oral	0781-2321ANDA
Aprepitant	aprepitant	capsule, oral	0781-2322ANDA
Aprepitant	aprepitant	capsule, oral	0781-2323ANDA
Aprepitant	aprepitant	kit	0781-4063ANDA
Armodafinil	Armodafinil	tablet, oral	0781-8029NDA AUTHORIZED GENERIC
Armodafinil	Armodafinil	tablet, oral	0781-8037NDA AUTHORIZED GENERIC
Armodafinil	Armodafinil	tablet, oral	0781-8045NDA AUTHORIZED GENERIC
Armodafinil	Armodafinil	tablet, oral	0781-8053NDA AUTHORIZED GENERIC
Arranon	nelarabine	injection, intravenous	66758-165NDA
Arsenic Trioxide	Arsenic Trioxide	injection, solution, intravenous	0781-3498ANDA
Azacitidine	Azacitidine	injection, powder, lyophilized, for solution, intravenous, subcutaneous	0781-3491ANDA
Azelaic Acid Gel	azelaic acid	gel, topical	0781-7172NDA AUTHORIZED GENERIC
Azelastine Hydrochloride	azelastine hydrochloride	solution/ drops, intraocular	61314-308ANDA
Azithromycin	Azithromycin	tablet, film coated, oral	0781-8089ANDA
Azithromycin	Azithromycin	tablet, film coated, oral	0781-8090ANDA
Azithromycin	Azithromycin	tablet, film coated, oral	0781-8091ANDA
Azopt	brinzolamide	suspension/ drops, ophthalmic	66758-085NDA
-	BIVALIRUDIN	powder	0781-3453DRUG FOR FURTHER PROCESSING
Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	tablet, film coated, oral	0185-0211ANDA
Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	tablet, film coated, oral	0185-0236ANDA
Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	tablet, film coated, oral	0185-0277ANDA
Benazepril Hydrochloride and Hydrochlorothiazide	Benazepril Hydrochloride and Hydrochlorothiazide	tablet, film coated, oral	0185-0325ANDA
Betaxolol Hydrochloride	Betaxolol Hydrochloride	solution/ drops, ophthalmic	61314-245NDA AUTHORIZED GENERIC
Bimatoprost	Bimatoprost	solution/ drops, ophthalmic	0781-6206ANDA
Brimonidine	brimonidine tartrate	solution/ drops, ophthalmic	0781-7177ANDA
Brimonidine Tartrate	Brimonidine Tartrate	solution, ophthalmic	61314-143ANDA
Brimonidine Tartrate	Brimonidine Tartrate	solution, ophthalmic	61314-144NDA
Brimonidine Tartrate and Timolol Maleate	Brimonidine Tartrate and Timolol Maleate	solution/ drops, ophthalmic	0781-7186ANDA
Brinzolamide	Brinzolamide	suspension/ drops, ophthalmic	0781-6014NDA AUTHORIZED GENERIC
Bromocriptine mesylate	Bromocriptine mesylate	tablet, oral	0781-5325ANDA
Bumetanide	Bumetanide	tablet, oral	0185-0128ANDA
Bumetanide	Bumetanide	tablet, oral	0185-0129ANDA
Bumetanide	Bumetanide	tablet, oral	0185-0130ANDA
Bumetanide	Bumetanide	tablet, oral	0781-8099ANDA
Bumetanide	Bumetanide	tablet, oral	0781-8113ANDA
Bumetanide	Bumetanide	tablet, oral	0781-8160ANDA
Butalbital, aspirin, and caffeine	Butalbital, aspirin, and caffeine	capsule, oral	0781-2270ANDA
CARMUSTINE	CARMUSTINE	kit	0781-3474ANDA
CASPOFUNGIN ACETATE	CASPOFUNGIN ACETATE	injection, powder, lyophilized, for solution, intravenous	0781-3421ANDA
CASPOFUNGIN ACETATE	CASPOFUNGIN ACETATE	injection, powder, lyophilized, for solution, intravenous	0781-3423ANDA
CILOXAN	ciprofloxacin hydrochloride	ointment, ophthalmic	66758-071NDA
CIMERLI	ranibizumab-eqrn	injection, solution, intravitreal	61314-624BLA
CIMERLI	ranibizumab-eqrn	injection, solution, intravitreal	61314-625BLA
CIPRO HC	ciprofloxacin hydrochloride and hydrocortisone	suspension/ drops, auricular (otic)	66758-087NDA
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5613NDA AUTHORIZED GENERIC
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5625NDA AUTHORIZED GENERIC
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5637NDA AUTHORIZED GENERIC
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5641NDA AUTHORIZED GENERIC
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5654NDA AUTHORIZED GENERIC
Carbidopa, Levodopa, and Entacapone	Carbidopa, Levodopa, and Entacapone	tablet, film coated, oral	0781-5669NDA AUTHORIZED GENERIC
Carteolol Hydrochloride	Carteolol Hydrochloride	solution, ophthalmic	61314-238ANDA
Cefazolin	Cefazolin	injection, powder, for solution, intramuscular, intravenous, parenteral	0781-3450ANDA
Cefazolin	Cefazolin	injection, powder, for solution, intramuscular, intravenous, parenteral	0781-3451ANDA
Cefazolin	Cefazolin	injection, powder, for solution, intravenous, parenteral	0781-3452ANDA
Cefdinir	Cefdinir	capsule, oral	0781-2176ANDA
Cefpodoxime Proxetil	Cefpodoxime Proxetil	tablet, film coated, oral	0781-5438ANDA
Cefpodoxime Proxetil	Cefpodoxime Proxetil	tablet, film coated, oral	0781-5439ANDA
Ceftriaxone Sodium	Ceftriaxone Sodium	injection, powder, for solution, intramuscular, intravenous	0781-3206ANDA
Ceftriaxone Sodium	Ceftriaxone Sodium	injection, powder, for solution, intramuscular, intravenous	0781-3207ANDA
Ceftriaxone Sodium	Ceftriaxone Sodium	injection, powder, for solution, intramuscular, intravenous	0781-3208ANDA
Ceftriaxone Sodium	Ceftriaxone Sodium	injection, powder, for solution, intramuscular, intravenous	0781-3209ANDA
Ceftriaxone Sodium	Ceftriaxone Sodium	injection, powder, for solution, intravenous	0781-3210ANDA
Cetirizine Hydrochloride	Cetirizine Hydrochloride	tablet, oral	0781-1684ANDA
Cetirizine Hydrochloride	Cetirizine Hydrochloride	tablet, chewable, oral	0781-5283ANDA
Cetirizine Hydrochloride	Cetirizine Hydrochloride	tablet, chewable, oral	0781-5284ANDA
Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	concentrate, oral	0781-4027ANDA
Chlorpromazine Hydrochloride	Chlorpromazine Hydrochloride	concentrate, oral	0781-4028ANDA
Ciprofloxacin Hydrochloride	Ciprofloxacin Hydrochloride	solution/ drops, ophthalmic	61314-656NDA AUTHORIZED GENERIC
Ciprofloxacin and Dexamethasone	ciprofloxacin and dexamethasone	suspension/ drops, auricular (otic)	0781-6186NDA AUTHORIZED GENERIC
Cladribine	Cladribine	tablet, oral	0781-8201ANDA
Clarithromycin	Clarithromycin	tablet, oral	0781-1961ANDA
Clarithromycin	Clarithromycin	tablet, oral	0781-1962ANDA
Clarithromycin	Clarithromycin	for suspension, oral	0781-6022ANDA
Clarithromycin	Clarithromycin	for suspension, oral	0781-6023ANDA
Clindamycin in 5 Percent Dextrose	Clindamycin in 5 Percent Dextrose	injection, solution, intravenous	0781-3288ANDA
Clindamycin in 5 Percent Dextrose	Clindamycin in 5 Percent Dextrose	injection, solution, intravenous	0781-3289ANDA
Clindamycin in 5 Percent Dextrose	Clindamycin in 5 Percent Dextrose	injection, solution, intravenous	0781-3290ANDA
Cosyntropin	Cosyntropin	injection, powder, lyophilized, for solution, intravenous	0781-3440ANDA
Cromolyn Sodium	Cromolyn Sodium	solution/ drops, ophthalmic	61314-237ANDA
Cyclopentolate Hydrochloride	Cyclopentolate Hydrochloride	solution, ophthalmic	61314-396ANDA
Cyclophosphamide	cyclophosphamide	injection, powder, for solution, intravenous, oral	0781-3233ANDA
Cyclophosphamide	cyclophosphamide	injection, powder, for solution, intravenous, oral	0781-3244ANDA
Cyclophosphamide	cyclophosphamide	injection, powder, for solution, intravenous, oral	0781-3255ANDA
Cyclophosphamide	Cyclophosphamide	injection, solution, concentrate, intravenous	0781-3528NDA
Cyclophosphamide	Cyclophosphamide	injection, solution, concentrate, intravenous	0781-3529NDA
Cyclophosphamide	Cyclophosphamide	injection, solution, concentrate, intravenous	0781-3530NDA
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	injection, intravenous	0781-3493ANDA
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	injection, intravenous	0781-3494ANDA
DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	DEXMEDETOMIDINE HYDROCHLORIDE IN 0.9% SODIUM CHLORIDE	injection, intravenous	0781-3495ANDA
DILUENT	water solution	injection, intravenous, subcutaneous	0781-6021ANDA
DORZOLAMIDE HYDROCHLORIDE	dorzolamide hydrochloride	solution/ drops, ophthalmic	61314-019ANDA
DUREZOL	difluprednate	emulsion, ophthalmic	66758-086NDA
Dapagliflozin	Dapagliflozin	tablet, film coated, oral	0781-5985ANDA

Neighbours

Registered in the same town

Novartis Pharmaceuticals CorporationKundl, AUT; Langkampfen, AUT · 2 sites
SGS North America Inc.Navi Mumbai, IND
Piramal Healthcare (Canada) LimitedNavi Mumbai, IND
Indoco Remedies LimitedNavi Mumbai, IND
Par Health USA, LLCNavi Mumbai, IND
Bioiberica SAUPalafolls, ESP
SITEC LABS LIMITEDNavi Mumbai, IND
INFAR SAPALAFOLLS, ESP
Jindal Drugs Private LimitedNavi Mumbai, IND
PADARSH PHARMACEUTICALS PRIVATE LIMITEDNavi Mumbai, IND
Reliance Life Sciences Private LimitedNavi Mumbai, IND
Riocare India Private LimitedNavi Mumbai, IND

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Enquiry

Common questions

Is Sandoz Industrial Products S.A FDA approved?: Sandoz Industrial Products S.A holds 5 FDA-registered establishments across 3 countries. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
Where are Sandoz Industrial Products S.A's drugs manufactured?: At registered sites in Austria, Spain, India. The FDA register lists Kundl; Langkampfen; Palafolls; Navi Mumbai. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging, relabelling, repackaging.
What drugs does Sandoz Industrial Products S.A make?: 441 products are listed under Sandoz Industrial Products S.A in the openFDA NDC Directory, most often as injection, solution; tablet, film coated; injection. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Are any Sandoz Industrial Products S.A products in shortage?: 11 presentations are currently listed in the FDA drug shortage database under Sandoz Industrial Products S.A, covering Amphetamine Aspartate Monohydrate, Amphetamine Sulfate, Dextroamphetamine Saccharate, Dextroamphetamine Sulfate Tablet, Clindamycin Phosphate Injection, Rocuronium Bromide Injection.

Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.