Topiramate 68462-0108
Product NDC
68462-0108- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 27, 2009
- Listing Expires
- December 31, 2027
- Application
- ANDA077627
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Topiramate | 25 mg/1 |
Drug Class
Cytochrome P450 2C19 Inhibitors [MoA]Cytochrome P450 3A4 Inducers [MoA]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(3)
500 TABLET, FILM COATED in 1 BOTTLE (68462-108-05)
1000 TABLET, FILM COATED in 1 BOTTLE (68462-108-10)
60 TABLET, FILM COATED in 1 BOTTLE (68462-108-60)