FDA NDC Directory · JSON-LD · Markdown

PROMETHEGAN

NDC 0713-0132 · HUMAN PRESCRIPTION DRUG · SUPPOSITORY

Generic namepromethazine hydrochloride
Labeler / ManufacturerCosette Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA087165
Dosage form / routeSUPPOSITORY · RECTAL
Active ingredientsPROMETHAZINE HYDROCHLORIDE (50 mg/1)
Marketing started19870831
Package count2

External sources

Source: openFDA. Public-domain (CC0).