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Data / Drug companies / Amneal Pharmaceuticals LLC

Amneal Pharmaceuticals LLC: 25 products in the FDA NDC directory, labeler code 64896

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

Amneal Pharmaceuticals LLC (labeler code 64896) lists 25 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 25 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on May 16, 2025.

The request: Watch Amneal Pharmaceuticals LLC (FDA labeler code 64896): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
64896
Products in commercial distribution
25
Packages
62
Finished drugs by generic name
7
Prescription products
25
Over the counter products
0
Controlled substance products
Schedule II 10
Flagged as original packager
23 of 23 products that carry the flag
Started marketing in the last 12 months
0
Earliest marketing start
August 2, 1976
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
New drug applications (NDA)1872%
Generic drugs (ANDA)728%

Products by type

TypeProductsShare
Prescription drugs25100%

Drugs it lists

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

Dosage forms

Dosage formProductsShare
Capsule, extended release1144%
Tablet, film coated, extended release728%
Granule312%
Capsule28%
Tablet, film coated14%
Injection14%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Brekiya64896-509InjectionNew drug applications (NDA)May 16, 2025
Crexont64896-970Capsule, extended releaseNew drug applications (NDA)August 9, 2024
Crexont64896-969Capsule, extended releaseNew drug applications (NDA)August 9, 2024
Crexont64896-968Capsule, extended releaseNew drug applications (NDA)August 9, 2024
Crexont64896-967Capsule, extended releaseNew drug applications (NDA)August 9, 2024
Ongentys64896-403CapsuleNew drug applications (NDA)April 5, 2024
Ongentys64896-402CapsuleNew drug applications (NDA)April 5, 2024
Lyvispah64896-078GranuleNew drug applications (NDA)June 1, 2023
Lyvispah64896-077GranuleNew drug applications (NDA)June 1, 2023
Lyvispah64896-076GranuleNew drug applications (NDA)June 1, 2023
Rytary64896-664Capsule, extended releaseNew drug applications (NDA)January 12, 2015
Rytary64896-663Capsule, extended releaseNew drug applications (NDA)January 12, 2015
Rytary64896-662Capsule, extended releaseNew drug applications (NDA)January 12, 2015
Rytary64896-661Capsule, extended releaseNew drug applications (NDA)January 12, 2015
Oxymorphone hydrochloride64896-701Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-700Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-699Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-698Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-697Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-696Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Oxymorphone hydrochloride64896-695Tablet, film coated, extended releaseGeneric drugs (ANDA)January 2, 2013
Albenza64896-693Tablet, film coatedNew drug applications (NDA)June 11, 1996
Dexedrine spansule64896-675Capsule, extended releaseNew drug applications (NDA)August 2, 1976
Dexedrine spansule64896-674Capsule, extended releaseNew drug applications (NDA)August 2, 1976
Dexedrine spansule64896-673Capsule, extended releaseNew drug applications (NDA)August 2, 1976

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.