FDA NDC Directory · JSON-LD · Markdown

Amoxicillin and Clavulanate Potassium

NDC 68788-4179 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065191
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (400 mg/5mL)
CLAVULANIC ACID (57 mg/5mL)
Marketing started20260731
Package count1

External sources

Source: openFDA. Public-domain (CC0).