Register entry

Advanz Pharma (US) Corp.

Data as of · How to read this entry

Registered sites
0
Active NDC listings
20
Live patents
0
Shortage listings
5
Countries
0
Alert

Drug shortage listings

5
DrugPresentationStatusAvailabilityPosted / updated
Nilutamide TabletOncologyNilandron, Tablet, 150 mg (NDC 59212-111-14)To Be Discontinued-1 Dec 20251 Dec 2025
Nilutamide TabletOncologyNilandron, Tablet, 150 mg (NDC 66993-212-38)To Be Discontinued-1 Dec 20251 Dec 2025
Phenoxybenzamine Hydrochloride CapsuleCardiovascularDibenzyline, Capsule, 10 mg (NDC 66993-066-02)To Be Discontinued-1 Dec 20251 Dec 2025
Phenoxybenzamine Hydrochloride CapsuleCardiovascularDibenzyline, Capsule, 10 mg (NDC 59212-001-01)To Be Discontinued-1 Dec 20251 Dec 2025
Phenoxybenzamine Hydrochloride CapsuleCardiovascularDibenzyline, Capsule, 10 mg (NDC 59212-001-02)To Be Discontinued-1 Dec 20251 Dec 2025
Catalogue

Drug listings by form and route

20

20 active NDC listings: 20 human prescription drug. By marketing category: NDA 17, UNAPPROVED DRUG OTHER 3.

Dosage formNDCs
tablet5
capsule4
tablet, film coated3
tablet, orally disintegrating3
elixir2
gel1
insert, extended release1
tablet, extended release1
RouteNDCs
oral18
topical1
vaginal1
Labeller name on the listingNDCs
advanz pharma (us) corp.20
Catalogue

Marketed products

20
BrandGeneric nameForm / routeNDC
Donnatalphenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromideelixir, oral59212-422UNAPPROVED DRUG OTHER
Donnatalphenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromideelixir, oral59212-423UNAPPROVED DRUG OTHER
DonnatalPHENOBARBITAL, HYOSCYAMINE SULFATE, ATROPINE SULFATE, SCOPOLAMINE HYDROBROMIDEtablet, oral59212-425UNAPPROVED DRUG OTHER
DyreniumTriamterenecapsule, oral59212-002NDA
DyreniumTriamterenecapsule, oral59212-003NDA
LANOXINdigoxintablet, oral59212-240NDA
LANOXINdigoxintablet, oral59212-242NDA
LANOXINdigoxintablet, oral59212-249NDA
NuvaRingetonogestrel and ethinyl estradiolinsert, extended release, vaginal59212-146NDA
Orapred ODTprednisolone sodium phosphatetablet, orally disintegrating, oral59212-700NDA
Orapred ODTprednisolone sodium phosphatetablet, orally disintegrating, oral59212-701NDA
Orapred ODTprednisolone sodium phosphatetablet, orally disintegrating, oral59212-702NDA
PANRETINalitretinoingel, topical59212-601NDA
PARNATEtranylcypromine sulfatetablet, film coated, oral59212-447NDA
PlaquenilHydroxychloroquine Sulfatetablet, oral59212-562NDA
SalagenPilocarpine Hydrochloridetablet, film coated, oral59212-705NDA
SalagenPilocarpine Hydrochloridetablet, film coated, oral59212-775NDA
UroxatralAlfuzosin HCltablet, extended release, oral59212-200NDA
ZonegranZonisamidecapsule, oral59212-680NDA
ZonegranZonisamidecapsule, oral59212-681NDA
Compare

Other companies listing digoxin

Enquiry

Common questions

Is Advanz Pharma (US) Corp. FDA approved?
Advanz Pharma (US) Corp. holds no registered establishment of its own; 20 drug products are listed under its name in the National Drug Code Directory, made at sites registered to other firms.
What drugs does Advanz Pharma (US) Corp. make?
20 products are listed under Advanz Pharma (US) Corp. in the openFDA NDC Directory, most often as tablet; capsule; tablet, film coated. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

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.