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acetaminophen pain reliever fever reducer

NDC 45802-730 · HUMAN OTC DRUG · SUPPOSITORY

Generic nameAcetaminophen
Labeler / ManufacturerPadagis Israel Pharmaceuticals Ltd
Marketing categoryAbbreviated NDA (generic) · App ANDA070608
Dosage form / routeSUPPOSITORY · RECTAL
Active ingredientsACETAMINOPHEN (650 mg/1)
Marketing started20101028
Marketing ended20261130
Package count4

External sources

Source: openFDA. Public-domain (CC0).