Topiramate
- Product NDC
- 70771-1858
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Topiramate
- Dosage form
- CAPSULE, EXTENDED RELEASE
- Route
- ORAL
- Labeler
- Zydus Lifesciences Limited
- Application
- ANDA207382
- Marketing category
- ANDA
- Substance
- TOPIRAMATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 70771-1858-1 | 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1858-1) | 2023-11-13 | | No | Historical |
| 70771-1858-3 | 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1858-3) | 2023-11-13 | | No | Historical |
| 70771-1858-5 | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (70771-1858-5) | 2023-11-13 | | No | Historical |
| 70771-1858-8 | 3 BLISTER PACK in 1 CARTON (70771-1858-8) / 10 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (70771-1858-2) | 2023-11-13 | | No | Historical |