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PROMETHAZINE HYDROCHLORIDE

NDC 68071-4424 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namepromethazine hydrochloride
Labeler / ManufacturerNuCare Pharmaceuticals,Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA040712
Dosage form / routeTABLET · ORAL
Active ingredientsPROMETHAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20060731
Package count3

External sources

Source: openFDA. Public-domain (CC0).