# Linezolid

NDC: 67877-419
Generic name: Linezolid
Labeler / Manufacturer: Ascend Laboratories, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20151221

FDA application: ANDA205517

## Active ingredients

- LINEZOLID: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67877-419"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67877-419
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7402aa01-50de-46c8-a341-d30da5b32b1c