Felbamate 70771-1077
Product NDC
70771-1077- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 15, 2017
- Listing Expires
- December 31, 2026
- Application
- ANDA208970
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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(5)
100 TABLET in 1 BOTTLE (70771-1077-1)
30 TABLET in 1 BOTTLE (70771-1077-3)
10 BLISTER PACK in 1 CARTON (70771-1077-4) / 10 TABLET in 1 BLISTER PACK
500 TABLET in 1 BOTTLE (70771-1077-5)
90 TABLET in 1 BOTTLE (70771-1077-9)