NDC 65162-735 – Felbamate
Felbamate 600 mg/1 · Tablet · Oral
Product NDC65162-735
Product details
- Brand name
- Felbamate
- Generic name
- Felbamate
- Labeler
- Amneal Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA201680
- Marketed since
- September 16, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Felbamate 600 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65162-735-03 | 30 TABLET in 1 BOTTLE (65162-735-03) | Sep 16, 2011 |
| 65162-735-09 | 90 TABLET in 1 BOTTLE (65162-735-09) | Sep 16, 2011 |
| 65162-735-18 | 180 TABLET in 1 BOTTLE (65162-735-18) | Sep 16, 2011 |
| 65162-735-27 | 270 TABLET in 1 BOTTLE (65162-735-27) | Sep 16, 2011 |
| 65162-735-50 | 500 TABLET in 1 BOTTLE (65162-735-50) | Sep 16, 2011 |
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