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Promethazine Hydrochloride

NDC 0904-7304 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA091179
Dosage form / routeTABLET · ORAL
Active ingredientsPROMETHAZINE HYDROCHLORIDE (25 mg/1)
Marketing started20230417
Package count1

External sources

Source: openFDA. Public-domain (CC0).