FDA NDC Directory · JSON-LD · Markdown

Linezolid

NDC 70518-4034 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA205517
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLINEZOLID (600 mg/1)
Marketing started20240508
Package count2

External sources

Source: openFDA. Public-domain (CC0).