# SIVEXTRO

NDC: 67919-041
Generic name: tedizolid phosphate
Labeler / Manufacturer: Merck Sharp & Dohme LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20140620

FDA application: NDA205435

## Active ingredients

- TEDIZOLID PHOSPHATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67919-041"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67919-041
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=75672079-589f-451a-bdbf-eaebcfcc80a9