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acetaminophen

NDC 72288-150 · HUMAN OTC DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAmazon.com Services LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA075077
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20260924
Package count1

External sources

Source: openFDA. Public-domain (CC0).