Topiramate 47335-0710
Product NDC
47335-0710- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 15, 2014
- Listing Expires
- December 31, 2027
- Application
- ANDA090278
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Topiramate | 50 mg/1 |
Drug Class
Cytochrome P450 2C19 Inhibitors [MoA]Cytochrome P450 3A4 Inducers [MoA]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(6)
100 TABLET, FILM COATED in 1 BOTTLE (47335-710-08)
500 TABLET, FILM COATED in 1 BOTTLE (47335-710-13)
1000 TABLET, FILM COATED in 1 BOTTLE (47335-710-18)
30 TABLET, FILM COATED in 1 BOTTLE (47335-710-83)
60 TABLET, FILM COATED in 1 BOTTLE (47335-710-86)
100 TABLET, FILM COATED in 1 BOTTLE (47335-710-88)