NDC 70771-1078 – Felbamate
Felbamate 600 mg/1 · Tablet · Oral
Product NDC70771-1078
Product details
- Brand name
- Felbamate
- Generic name
- Felbamate
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA208970
- Marketed since
- August 15, 2017
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Felbamate 600 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 70771-1078-1 | 100 TABLET in 1 BOTTLE (70771-1078-1) | Aug 15, 2017 |
| 70771-1078-3 | 30 TABLET in 1 BOTTLE (70771-1078-3) | Aug 15, 2017 |
| 70771-1078-4 | 10 BLISTER PACK in 1 CARTON (70771-1078-4) / 10 TABLET in 1 BLISTER PACK | Aug 15, 2017 |
| 70771-1078-5 | 500 TABLET in 1 BOTTLE (70771-1078-5) | Aug 15, 2017 |
| 70771-1078-8 | 180 TABLET in 1 BOTTLE (70771-1078-8) | Aug 15, 2017 |
| 70771-1078-9 | 90 TABLET in 1 BOTTLE (70771-1078-9) | Aug 15, 2017 |
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