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Promethazine

NDC 54348-117 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namePROMETHAZINE
Labeler / ManufacturerPharmPak, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040712
Dosage form / routeTABLET · ORAL
Active ingredientsPROMETHAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20190711
Package count10

External sources

Source: openFDA. Public-domain (CC0).