NDC 68382-141 – Topiramate
Topiramate 200 mg/1 · Tablet, Film Coated · Oral
Product NDC68382-141
Product details
- Brand name
- Topiramate
- Generic name
- Topiramate
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078235
- Marketed since
- March 27, 2009
- Listing expires
- December 31, 2027
Active ingredients
- Topiramate 200 mg/1
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 68382-141-01 | 100 TABLET, FILM COATED in 1 BOTTLE (68382-141-01) | Mar 27, 2009 |
| 68382-141-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68382-141-05) | Mar 27, 2009 |
| 68382-141-14 | 60 TABLET, FILM COATED in 1 BOTTLE (68382-141-14) | Mar 27, 2009 |
| 68382-141-16 | 90 TABLET, FILM COATED in 1 BOTTLE (68382-141-16) | Mar 27, 2009 |
Recalls mentioning this NDC
- D-0015-2015 Oct 22, 2014 · Class II
Presence of Foreign Tablets: Presence of topiramate 100 mg tablets comingled with 200 mg tablets.
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