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Acetaminophen

NDC 53329-643 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerMedline Industries, LP
Marketing categoryAbbreviated NDA (generic) · App ANDA076200
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20020430
Marketing ended20261231
Package count1

External sources

Source: openFDA. Public-domain (CC0).