Zonisamide 62756-0259
Product NDC
62756-0259- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Capsule
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 17, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA077634
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Zonisamide | 50 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Carbonic Anhydrase Inhibitors [MoA]
Packaging Options(4)
30 CAPSULE in 1 BOTTLE (62756-259-01)
100 CAPSULE in 1 BOTTLE (62756-259-02)
100 CAPSULE in 1 BOTTLE (62756-259-03)
1000 CAPSULE in 1 BOTTLE (62756-259-04)