SIVEXTRO 200 mg/1
tedizolid phosphate · TABLET, FILM COATED · Merck Sharp & Dohme LLC
No Recall History
Plain English
SIVEXTRO is a tablet, film coated containing tedizolid phosphate at 200 mg/1, taken oral. Manufactured by Merck Sharp & Dohme LLC.
Key Facts
- Brand Name
- SIVEXTRO
- Generic Name
- tedizolid phosphate
- NDC Code (Product)
67919-041- Manufacturer
- Merck Sharp & Dohme LLC
- Strength
- 200 mg/1
- Dosage Form
- TABLET, FILM COATED
- Route
- ORAL
- Marketing Status
- Application #
- NDA205435
- Marketing Start
- 06/20/2014
Recall History
No Recall HistoryFrequently Asked Questions
What is SIVEXTRO used for?
SIVEXTRO contains tedizolid phosphate. It is a tablet, film coated taken oral. Consult your doctor for specific uses.
Is SIVEXTRO a controlled substance?
SIVEXTRO is not classified as a controlled substance by the DEA.
What is the generic name for SIVEXTRO?
The generic name for SIVEXTRO is tedizolid phosphate. There are no other listed brand versions of tedizolid phosphate.
What is the NDC code for SIVEXTRO 200 mg/1?
The NDC (National Drug Code) for SIVEXTRO 200 mg/1 is 67919-041, listed by Merck Sharp & Dohme LLC.
Other SIVEXTRO Dosages
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)