71090-001 : Keveyis 50 mg Oral Tablet
| NDC: | 71090-001 |
| Labeler: | Strongbridge Us Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: | Keveyis |
| Dosage Form: | Oral Tablet |
| Application #: | NDA011366 |
| Rev. Date: |
Appearance:
| Markings: | D;50 |
| Shapes: |
Round |
| Colors: |
 White |
| Size (mm): | 6 |
| Segments: * | 2 |
* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 2 indicates a scored pill which can be broken into 2 equal pieces. | |
NDC Package Codes:
- 71090-001-01: 100 TABLET IN 1 BOTTLE (71090‑001‑01)
Active Ingredients:
- Dichlorphenamide
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Lactose Monohydrate
- Magnesium Stearate
- Starch, Corn
Pharmaceutical Classes:
- Carbonic Anhydrase Inhibitors [MoA]
- Sulfonamides [CS]
- Carbonic Anhydrase Inhibitor [EPC]
Related Products:
Based on records with the same trade name.- 51672-4177 Keveyis 50 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
- 72065-001 Keveyis 50 mg Oral Tablet by Xeris Pharmaceuticals, Inc.
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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.
