Felbamate 51672-4185
Product NDC
51672-4185- Manufacturer
- Taro Pharmaceuticals U.s.a., Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 20, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA207093
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Felbamate | 400 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(3)
100 TABLET in 1 BOTTLE (51672-4185-1)
90 TABLET in 1 BOTTLE (51672-4185-5)
30 TABLET in 1 BOTTLE (51672-4185-6)