NDC 47335-710 – Topiramate
Topiramate 50 mg/1 · Tablet, Film Coated · Oral
Product NDC47335-710
Product details
- Brand name
- Topiramate
- Generic name
- Topiramate
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA090278
- Marketed since
- December 15, 2014
- Listing expires
- December 31, 2027
Active ingredients
- Topiramate 50 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 47335-710-08 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-710-08) | Dec 15, 2014 |
| 47335-710-13 | 500 TABLET, FILM COATED in 1 BOTTLE (47335-710-13) | Dec 15, 2014 |
| 47335-710-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (47335-710-18) | Dec 15, 2014 |
| 47335-710-83 | 30 TABLET, FILM COATED in 1 BOTTLE (47335-710-83) | Dec 15, 2014 |
| 47335-710-86 | 60 TABLET, FILM COATED in 1 BOTTLE (47335-710-86) | Dec 15, 2014 |
| 47335-710-88 | 100 TABLET, FILM COATED in 1 BOTTLE (47335-710-88) | Dec 15, 2014 |
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