NDC 72162-1770 – Felbamate
Felbamate 400 mg/1 · Tablet · Oral
Product NDC72162-1770
Product details
- Brand name
- Felbamate
- Generic name
- Felbamate
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA202284
- Marketed since
- September 4, 2018
- Listing expires
- December 31, 2027
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Felbamate 400 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 72162-1770-1 | 100 TABLET in 1 BOTTLE (72162-1770-1) | Mar 25, 2026 |
Other Felbamate products
- 65162-734 Felbamate 400 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 65162-735 Felbamate 600 mg/1 · Tablet · Amneal Pharmaceuticals LLC
- 53746-734 Felbamate 400 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 53746-735 Felbamate 600 mg/1 · Tablet · Amneal Pharmaceuticals of New York LLC
- 62559-730 Felbamate 400 mg/1 · Tablet · ANI Pharmaceuticals, Inc.
- 62559-731 Felbamate 600 mg/1 · Tablet · ANI Pharmaceuticals, Inc.
- 63629-1937 Felbamate 400 mg/1 · Tablet · Bryant Ranch Prepack
- 63629-1944 Felbamate 600 mg/1 · Tablet · Bryant Ranch Prepack
- 72162-1771 Felbamate 600 mg/1 · Tablet · Bryant Ranch Prepack
- 51672-4185 Felbamate 400 mg/1 · Tablet · Sun Pharmaceutical Industries, Inc.
- 51672-4186 Felbamate 600 mg/1 · Tablet · Sun Pharmaceutical Industries, Inc.
- 72578-057 Felbamate 600 mg/1 · Tablet · Viona Pharmaceuticals Inc