NDC 68462-153 – Topiramate
Topiramate 50 mg/1 · Tablet, Film Coated · Oral
Product NDC68462-153
Product details
- Brand name
- Topiramate
- Generic name
- Topiramate
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077627
- Marketed since
- March 27, 2009
- Listing expires
- December 31, 2027
Active ingredients
- Topiramate 50 mg/1
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 68462-153-05 | 500 TABLET, FILM COATED in 1 BOTTLE (68462-153-05) | Jul 30, 2020 |
| 68462-153-10 | 1000 TABLET, FILM COATED in 1 BOTTLE (68462-153-10) | Mar 27, 2009 |
| 68462-153-60 | 60 TABLET, FILM COATED in 1 BOTTLE (68462-153-60) | Mar 27, 2009 |
Recalls mentioning this NDC
- D-331-2013 May 22, 2013 · Class III
Chemical Contamination: Topiramate Tablets is being recalled due to complaints related to an off - odor. described as moldy, musty or fishy in nature.
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