FDA NDC Directory · JSON-LD · Markdown

Amoxicillin

NDC 68788-8731 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA065119
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (400 mg/5mL)
Marketing started20240916
Package count1

External sources

Source: openFDA. Public-domain (CC0).