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Promethazine Hydrochloride

NDC 70518-1306 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA040596
Dosage form / routeTABLET · ORAL
Active ingredientsPROMETHAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20180716
Package count3

External sources

Source: openFDA. Public-domain (CC0).