FDA NDC Directory · JSON-LD · Markdown

Promethazine Hydrochloride and Dextromethorphan Hydrobromide

NDC 27808-057 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerCranbury Pharmaceuticals, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091687
Dosage form / routeSOLUTION · ORAL
Active ingredientsDEXTROMETHORPHAN HYDROBROMIDE (15 mg/5mL)
PROMETHAZINE HYDROCHLORIDE (6.25 mg/5mL)
Marketing started20140131
Marketing ended20270401
Package count1

External sources

Source: openFDA. Public-domain (CC0).