66490-690 : Mysoline 50 mg Oral Tablet
| NDC: | 66490-690 |
| Labeler: | Valeant Pharmaceuticals North America |
| Product Type: | Human Prescription Drug |
| Drug Name: |  Mysoline |
| Dosage Form: | Oral Tablet |
| Application #: | NDA009170 |
| Rev. Date: |
Appearance:
| Markings: | MYSOLINE;50;M |
| Shapes: |
Square (4 sides) |
| 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. | |
The above image is provided by the U.S. National Library of Medicine (NLM) and is not part of the official label.
NDC Package Codes:
- 66490-690-10: 100 TABLET IN 1 BOTTLE (66490‑690‑10)
Active Ingredients:
- Primidone
Dosage Strength:
- 50 mg
Inactive Ingredients:
- Cellulose, Microcrystalline
- Lactose Monohydrate
- Methylcellulose (15 Cps)
- Sodium Starch Glycolate Type a Potato
- Talc
- Sodium Lauryl Sulfate
- Magnesium Stearate
Pharmaceutical Classes:
- Anti-epileptic Agent [EPC]
- Decreased Central Nervous System Disorganized Electrical Activity [PE]
Related Products:
Based on records with the same trade name.- 66490-691 Mysoline 250 mg Oral Tablet by Valeant Pharmaceuticals North America
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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.