FDA NDC Directory · JSON-LD · Markdown

Pain Relief

NDC 41250-802 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameAcetaminophen
Labeler / ManufacturerMeijer Distribution Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA075077
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20170303
Package count2

External sources

Source: openFDA. Public-domain (CC0).