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Data / Drug companies / Patrin Pharma, Inc.

Patrin Pharma, Inc.: 24 products in the FDA NDC directory, labeler code 39328

Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).

Patrin Pharma, Inc. (labeler code 39328) lists 24 products in the FDA National Drug Code Directory, covering 13 finished drugs by generic name. By type: 16 prescription drugs, 8 over the counter drugs. Its main marketing category is over the counter monograph drugs. The newest product started marketing on October 1, 2025.

The request: Watch Patrin Pharma, Inc. (FDA labeler code 39328): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
39328
Products in commercial distribution
24
Packages
39
Finished drugs by generic name
13
Prescription products
16
Over the counter products
8
Controlled substance products
Schedule II 2, Schedule V 1
Flagged as original packager
24 of 24 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
April 1, 2013
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Over the counter monograph drugs833.3%
Other unapproved drugs833.3%
Generic drugs (ANDA)833.3%

Products by type

TypeProductsShare
Prescription drugs1666.7%
Over the counter drugs833.3%

Drugs it lists

Finished drugs by generic name, with how many companies list each.

Dosage forms

Dosage formProductsShare
Solution729.2%
Syrup312.5%
Liquid312.5%
Tablet312.5%
Cream312.5%
Suppository28.3%
Tablet, extended release14.2%
Tablet, orally disintegrating14.2%
Oil14.2%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Urea 40%39328-019CreamOther unapproved drugsOctober 1, 2025
Hyoscyamine Sulfate39328-052Tablet, extended releaseOther unapproved drugsAugust 16, 2024
Hyoscyamine Sulfate39328-051TabletOther unapproved drugsAugust 15, 2024
Hyoscyamine Sulfate39328-050TabletOther unapproved drugsAugust 15, 2024
Hyoscyamine Sulfate39328-049Tablet, orally disintegratingOther unapproved drugsAugust 15, 2024
Levetiracetam39328-511SolutionGeneric drugs (ANDA)January 31, 2024
Acetaminophen Solution39328-034LiquidOver the counter monograph drugsOctober 16, 2023
Senna UD39328-220SyrupOver the counter monograph drugsOctober 1, 2023
Senna UD39328-120SyrupOver the counter monograph drugsOctober 1, 2023
Senna39328-020SyrupOver the counter monograph drugsOctober 1, 2023
Acetaminophen Solution39328-032LiquidOver the counter monograph drugsSeptember 27, 2023
Acetaminophen Solution39328-031LiquidOver the counter monograph drugsSeptember 27, 2023
Calcitriol39328-042SolutionGeneric drugs (ANDA)August 14, 2023
Amantadine Hydrochloride39328-530SolutionGeneric drugs (ANDA)August 11, 2023
Pregabalin39328-090SolutionGeneric drugs (ANDA)June 14, 2022
Cyproheptadine Hydrochloride39328-544SolutionGeneric drugs (ANDA)February 15, 2022
Hydrocortisone Acetate39328-129SuppositoryOther unapproved drugsJanuary 1, 2022
Hydrocortisone Acetate39328-029SuppositoryOther unapproved drugsJanuary 1, 2022
Methylphenidate HCl39328-154SolutionGeneric drugs (ANDA)April 23, 2020
Methylphenidate HCl39328-054SolutionGeneric drugs (ANDA)April 23, 2020
Lidocaine Anorectal39328-025CreamOver the counter monograph drugsNovember 1, 2018
Lidocaine39328-024CreamOver the counter monograph drugsNovember 1, 2018
Flac Otic Oil39328-079OilGeneric drugs (ANDA)April 12, 2018
Prenatal Plus Vitamins39328-106TabletOther unapproved drugsApril 1, 2013

CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.