FDA NDC Directory · JSON-LD · Markdown

Linezolid

NDC 67877-419 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAscend Laboratories, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA205517
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsLINEZOLID (600 mg/1)
Marketing started20151221
Package count8

External sources

Source: openFDA. Public-domain (CC0).