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Acetaminophen

NDC 69842-635 · HUMAN OTC DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerCVS Pharmacy, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207229
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20221013
Package count1

External sources

Source: openFDA. Public-domain (CC0).