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Data / Drug companies / USAntibiotics, LLC

USAntibiotics, LLC: 10 products in the FDA NDC directory, labeler code 81964

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

USAntibiotics, LLC (labeler code 81964) lists 10 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 10 prescription drugs. Its main marketing category is authorized generics (NDA). The newest product started marketing on December 15, 2025.

The request: Watch USAntibiotics, LLC (FDA labeler code 81964): each new product listing and each discontinued product. $10 of work on sign-up, no card.

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Labeler code
81964
Products in commercial distribution
10
Packages
28
Finished drugs by generic name
2
Prescription products
10
Over the counter products
0
Flagged as original packager
7 of 7 products that carry the flag
Started marketing in the last 12 months
1
Earliest marketing start
July 15, 2022
openFDA record search
api.fda.gov

Products by marketing category

Share of the company's products in commercial distribution.

Marketing categoryProductsShare
Authorized generics (NDA)660%
Generic drugs (ANDA)330%
New drug applications (NDA)110%

Products by type

TypeProductsShare
Prescription drugs10100%

Drugs it lists

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

DrugProductsCompanies listing it
Amoxicillin and clavulanate potassium635
Amoxicillin435

Dosage forms

Dosage formProductsShare
For suspension550%
Capsule330%
Tablet, coated110%
Tablet, film coated, extended release110%

Pharmacologic classes

FDA established pharmacologic classes of its products.

Newest products

By marketing start date.

ProductProduct NDCDosage formMarketing categoryMarketing start
Amoxicillin and Clavulanate Potassium81964-220Tablet, film coated, extended releaseAuthorized generics (NDA)December 15, 2025
Amoxicillin81964-350CapsuleGeneric drugs (ANDA)May 15, 2025
Amoxicillin81964-207For suspensionAuthorized generics (NDA)April 1, 2024
Amoxicillin and clavulanate potassium81964-212For suspensionAuthorized generics (NDA)December 5, 2022
Amoxicillin and clavulanate potassium81964-204For suspensionAuthorized generics (NDA)December 5, 2022
Amoxicillin and clavulanate potassium81964-221Tablet, coatedAuthorized generics (NDA)November 21, 2022
Amoxicillin and clavulanate potassium81964-203For suspensionAuthorized generics (NDA)September 19, 2022
Amoxicillin81964-225CapsuleGeneric drugs (ANDA)September 15, 2022
Amoxicillin81964-205CapsuleGeneric drugs (ANDA)September 15, 2022
Augmentin es-60081964-003For suspensionNew drug applications (NDA)July 15, 2022

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.