49938-110 : Ruzurgi 10 mg Oral Tablet
| NDC: | 49938-110 |
| Labeler: | Jacobus Pharmaceutical Company, Inc. |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Ruzurgi |
| Dosage Form: | Oral Tablet |
| Application #: | NDA209321 |
| Rev. Date: |
Appearance:
| Markings: | JACOBUS;10;110 |
| Shapes: |
Oval |
| Colors: |
 White |
| Size (mm): | 11 |
| 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:
- 49938-110-01: 1 BOTTLE, PLASTIC IN 1 CARTON (49938‑110‑01) > 100 TABLET IN 1 BOTTLE, PLASTIC
Active Ingredients:
- Amifampridine
Dosage Strength:
- 10 mg
Inactive Ingredients:
- Silicon Dioxide
- Dibasic Calcium Phosphate Dihydrate
- Magnesium Stearate
- Microcrystalline Cellulose 101
- Sodium Starch Glycolate Type a Potato /
Pharmaceutical Classes:
- Potassium Channel Antagonists [MoA]
- Potassium Channel Blocker [EPC]
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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.