Pretomanid 200 mg/1
Pretomanid · TABLET · Viatris Specialty LLC
No Recall History
Plain English
Pretomanid is a tablet containing pretomanid at 200 mg/1, taken oral. Manufactured by Viatris Specialty LLC.
Key Facts
- Brand Name
- Pretomanid
- Generic Name
- Pretomanid
- NDC Code (Product)
49502-476- Manufacturer
- Viatris Specialty LLC
- Strength
- 200 mg/1
- Dosage Form
- TABLET
- Route
- ORAL
- Marketing Status
- Application #
- NDA212862
- Drug Class
- Antimycobacterial [EPC]
- Marketing Start
- 11/07/2019
Recall History
No Recall HistoryFrequently Asked Questions
What is Pretomanid used for?
Pretomanid contains Pretomanid. It is a tablet taken oral. Consult your doctor for specific uses.
Is Pretomanid a controlled substance?
Pretomanid is not classified as a controlled substance by the DEA.
What is the generic name for Pretomanid?
The generic name for Pretomanid is Pretomanid. There are no other listed brand versions of Pretomanid.
What is the NDC code for Pretomanid 200 mg/1?
The NDC (National Drug Code) for Pretomanid 200 mg/1 is 49502-476, listed by Viatris Specialty LLC.
Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.
Data from openFDA · Public domain (CC0 1.0)