Tiagabine Hydrochloride 62756-0224
Product NDC
62756-0224- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 4, 2011
- Listing Expires
- December 31, 2026
- Application
- ANDA077555
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tiagabine Hydrochloride | 4 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (62756-224-08)
1000 TABLET, FILM COATED in 1 BOTTLE (62756-224-18)
30 TABLET, FILM COATED in 1 BOTTLE (62756-224-83)
100 TABLET, FILM COATED in 1 BOTTLE (62756-224-88)