FDA NDC Directory · JSON-LD · Markdown

Amoxicillin

NDC 65862-070 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerAurobindo Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA065334
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (200 mg/5mL)
Marketing started20061228
Package count3

External sources

Source: openFDA. Public-domain (CC0).