Is Patrin Pharma, Inc FDA approved?

Patrin Pharma, Inc holds 1 FDA-registered establishment in the United States. 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 Patrin Pharma, Inc's drugs manufactured?

The FDA register lists Niles, IL. Registered operations: labelling, finished drug manufacture.

What drugs does Patrin Pharma, Inc make?

24 products are listed under Patrin Pharma, Inc in the openFDA NDC Directory, most often as solution; cream; liquid. The full breakdown by dosage form and route is above. A listing count is not a sales figure.

Patrin Pharma, Inc

Data as of 24 Sept 2026 · How to read this entry

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Registered sites: 1
Active NDC listings: 24
Labeller names: 3
Live patents: 0
Countries: 1
Base: United States

Authorisation

Registered operations

Labelling1Finished drug manufacture1

Sites

Registered establishments

Establishment	Address	Registered for	FEI / DUNS
Patrin Pharma, Inc	5603 W Howard St, Niles, Illinois (IL) 60714-4011, United States (USA)	Labelling, Finished drug manufacture	3006557630806841677

Catalogue

Drug listings by form and route

24 active NDC listings: 16 human prescription drug, 8 human otc drug. By marketing category: ANDA 8, OTC MONOGRAPH DRUG 8, UNAPPROVED DRUG OTHER 8.

Dosage form	NDCs
solution	7
cream	3
liquid	3
syrup	3
tablet	3
suppository	2
oil	1
tablet, extended release	1
tablet, orally disintegrating	1

Route	NDCs
oral	17
rectal	3
topical	2
auricular (otic)	1
sublingual	1

Labeller name on the listing	NDCs
patrin pharma, inc.	18
patrin pharma inc.	3
patrin pharma, inc	3

Catalogue

Marketed products

Brand	Generic name	Form / route	NDC
Acetaminophen Solution	Acetaminophen	liquid, oral	39328-031OTC MONOGRAPH DRUG
Acetaminophen Solution	Acetaminophen	liquid, oral	39328-032OTC MONOGRAPH DRUG
Acetaminophen Solution	Acetaminophen	liquid, oral	39328-034OTC MONOGRAPH DRUG
Amantadine Hydrochloride	amantadine hydrochloride	solution, oral	39328-530ANDA
Calcitriol	Calcitriol	solution, oral	39328-042ANDA
Cyproheptadine Hydrochloride	Cyproheptadine Hydrochloride	solution, oral	39328-544ANDA
Flac Otic Oil	fluocinolone acetonide	oil, auricular (otic)	39328-079ANDA
Hydrocortisone Acetate	Hydrocortisone Acetate	suppository, rectal	39328-029UNAPPROVED DRUG OTHER
Hydrocortisone Acetate	Hydrocortisone Acetate	suppository, rectal	39328-129UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, orally disintegrating, oral	39328-049UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, oral	39328-050UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, sublingual	39328-051UNAPPROVED DRUG OTHER
Hyoscyamine Sulfate	Hyoscyamine Sulfate	tablet, extended release, oral	39328-052UNAPPROVED DRUG OTHER
Levetiracetam	Levetiracetam	solution, oral	39328-511ANDA
Lidocaine	Lidocaine	cream, topical	39328-024OTC MONOGRAPH DRUG
Lidocaine Anorectal	Lidocaine	cream, rectal	39328-025OTC MONOGRAPH DRUG
Methylphenidate HCl	Methylphenidate HCl	solution, oral	39328-054ANDA
Methylphenidate HCl	Methylphenidate HCl	solution, oral	39328-154ANDA
PREGABALIN	PREGABALIN	solution, oral	39328-090ANDA
Prenatal Plus Vitamins	prenatal with ferrous fumarate and folic acid	tablet, oral	39328-106UNAPPROVED DRUG OTHER
Senna	Sennosides	syrup, oral	39328-020OTC MONOGRAPH DRUG
Senna UD	Sennosides	syrup, oral	39328-120OTC MONOGRAPH DRUG
Senna UD	Sennosides	syrup, oral	39328-220OTC MONOGRAPH DRUG
Urea 40%	Urea	cream, topical	39328-019UNAPPROVED DRUG OTHER

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Enquiry

Common questions

Is Patrin Pharma, Inc FDA approved?: Patrin Pharma, Inc holds 1 FDA-registered establishment in the United States. 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 Patrin Pharma, Inc's drugs manufactured?: The FDA register lists Niles, IL. Registered operations: labelling, finished drug manufacture.
What drugs does Patrin Pharma, Inc make?: 24 products are listed under Patrin Pharma, Inc in the openFDA NDC Directory, most often as solution; cream; liquid. 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.