FDA NDC Directory · JSON-LD · Markdown

Medline

NDC 53329-221 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Generic nameAcetaminophen
Labeler / ManufacturerMedline Industries, LP
Marketing categoryAbbreviated NDA (generic) · App ANDA075077
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20260828
Package count1

External sources

Source: openFDA. Public-domain (CC0).