FDA NDC
SIVEXTRO
This name is from the loaded FDA file.
Source: FDA NDC Directory, live from openFDA. Publisher page
- NDC
- 67919-041
- Proprietary name
- SIVEXTRO
- Nonproprietary name
- tedizolid phosphate
- Labeler
- Merck Sharp & Dohme LLC
- Dosage form
- TABLET, FILM COATED
- Strength
- 200 mg/1
HCPCS J0695 Billable units per 11-digit NDC: 200.