FDA NDC Directory · JSON-LD · Markdown

Linezolid

NDC 57664-683 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namelinezolid
Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA207354
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsLINEZOLID (600 mg/300mL)
Marketing started20170201
Package count1

External sources

Source: openFDA. Public-domain (CC0).