FDA NDC Directory · JSON-LD · Markdown

Arthritis Pain

NDC 57344-200 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameAcetaminophen
Labeler / ManufacturerAAA Pharmaceutical, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211544
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20250912
Package count1

External sources

Source: openFDA. Public-domain (CC0).