FDA NDC Directory · JSON-LD · Markdown

Amoxicillin and Clavulanate Potassium

NDC 42571-164 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA205187
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsAMOXICILLIN (400 mg/5mL)
CLAVULANATE POTASSIUM (57 mg/5mL)
Marketing started20210701
Package count1

External sources

Source: openFDA. Public-domain (CC0).