49502-476 : Pretomanid 200 mg Oral Tablet
| NDC: | 49502-476 |
| Labeler: | Mylan Specialty L.p. |
| Product Type: | Human Prescription Drug |
| Drug Name: | Pretomanid |
| Dosage Form: | Oral Tablet |
| Application #: | NDA212862 |
| Rev. Date: |
Appearance:
| Markings: | M;P200 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 18 |
| Segments: * | 1 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines. | |
NDC Package Codes:
- 49502-476-26: 26 TABLET IN 1 BOTTLE (49502‑476‑26)
Active Ingredients:
- Pretomanid
Dosage Strength:
- 200 mg
Inactive Ingredients:
- Lactose Monohydrate
- Microcrystalline Cellulose
- Sodium Starch Glycolate Type a Potato
- Magnesium Stearate
- Silicon Dioxide
- Sodium Lauryl Sulfate
- Povidone, Unspecified /
NDC QR Code
Scan the QR code below to easily reference this data in the future:
< Prev: 49502-475Next: 49502-500 >
Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.
