NDC 70710-1287 – vigabatrin
Vigabatrin 500 mg/1 · Tablet, Film Coated · Oral
Product NDC70710-1287
Product details
- Brand name
- vigabatrin
- Generic name
- vigabatrin
- Labeler
- Zydus Pharmaceuticals (USA) Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA215707
- Marketed since
- January 20, 2022
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Vigabatrin 500 mg/1
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 70710-1287-1 | 100 TABLET, FILM COATED in 1 BOTTLE (70710-1287-1) | Jan 20, 2022 |
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