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Acetaminophen

NDC 11822-5091 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerRITE AID
Marketing categoryAbbreviated NDA (generic) · App ANDA211544
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20241101
Package count2

External sources

Source: openFDA. Public-domain (CC0).