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Data / Drug companies / FH2 Pharma LLC

FH2 Pharma LLC: 9 products in the FDA NDC directory, labeler code 72887

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

FH2 Pharma LLC (labeler code 72887) lists 9 products in the FDA National Drug Code Directory, covering 6 finished drugs by generic name. By type: 9 prescription drugs. Its main marketing category is generic drugs (ANDA). The newest product started marketing on August 30, 2024.

The request: Watch FH2 Pharma LLC (FDA labeler code 72887): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
72887
Products in commercial distribution
9
Packages
9
Finished drugs by generic name
6
Prescription products
9
Over the counter products
0
Controlled substance products
Schedule II 5
Flagged as original packager
9 of 9 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
June 3, 2019
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Generic drugs (ANDA)9100%

Products by type

TypeProductsShare
Prescription drugs9100%

Drugs it lists

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

DrugProductsCompanies listing it
Oxycodone and acetaminophen tablets21
Ursodiol228
Oxycodone and acetaminophen232
Methocarbamol167
Oxycodone hydrochloride and acetaminophen16
Glycopyrrolate164

Dosage forms

Dosage formProductsShare
Tablet555.6%
Capsule222.2%
Tablet, film coated111.1%
Solution111.1%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Methocarbamol72887-873Tablet, film coatedGeneric drugs (ANDA)August 30, 2024
Glycopyrrolate72887-160TabletGeneric drugs (ANDA)November 29, 2021
Ursodiol 400 mg72887-144CapsuleGeneric drugs (ANDA)November 18, 2021
Ursodiol 200 mg72887-143CapsuleGeneric drugs (ANDA)November 18, 2021
Oxycodone and acetaminophen72887-682TabletGeneric drugs (ANDA)March 2, 2021
Oxycodone and acetaminophen72887-681TabletGeneric drugs (ANDA)September 25, 2020
Oxycodone and acetaminophen72887-683TabletGeneric drugs (ANDA)July 1, 2020
Oxycodone hydrochloride and acetaminophen72887-648SolutionGeneric drugs (ANDA)March 1, 2020
Oxycodone and acetaminophen72887-193TabletGeneric drugs (ANDA)June 3, 2019

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.