FDA NDC Directory · JSON-LD · Markdown

vecuronium bromide

NDC 47335-931 · HUMAN PRESCRIPTION DRUG · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079001
Dosage form / routeINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION · INTRAVENOUS
Active ingredientsVECURONIUM BROMIDE (1 mg/mL)
Marketing started20141215
Package count1

External sources

Source: openFDA. Public-domain (CC0).