Topiramate
- Product NDC
- 47335-712
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Topiramate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Application
- ANDA090278
- Marketing category
- ANDA
- Substance
- TOPIRAMATE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 47335-712-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-08) | 2014-12-15 | | No | Historical |
| 47335-712-13 | 500 TABLET, FILM COATED in 1 BOTTLE (47335-712-13) | 2014-12-15 | | No | Historical |
| 47335-712-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18) | 2014-12-15 | | No | Historical |
| 47335-712-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-712-83) | 2014-12-15 | | No | Historical |
| 47335-712-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-712-86) | 2014-12-15 | | No | Historical |
| 47335-712-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-88) | 2014-12-15 | | No | Historical |