FDA NDC Directory · JSON-LD · Markdown

Chlorzoxazone

NDC 51862-339 · HUMAN PRESCRIPTION DRUG · TABLET

Generic namechlorzoxazone
Labeler / ManufacturerMayne Pharma Commercial LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA211849
Dosage form / routeTABLET · ORAL
Active ingredientsCHLORZOXAZONE (500 mg/1)
Marketing started20200731
Package count1

External sources

Source: openFDA. Public-domain (CC0).