NDC 68788-7568 – Topiramate
Topiramate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-7568
Product details
- Brand name
- Topiramate
- Generic name
- Topiramate
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078235
- Marketed since
- March 27, 2009
- Listing expires
- December 31, 2026
Active ingredients
- Topiramate 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68788-7568-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-7568-3) | Dec 27, 2019 |
| 68788-7568-5 | 15 TABLET, FILM COATED in 1 BOTTLE (68788-7568-5) | Dec 27, 2019 |
| 68788-7568-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-7568-6) | Dec 27, 2019 |
| 68788-7568-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-7568-9) | Dec 27, 2019 |
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