NDC 0093-8072 – Tiagabine Hydrochloride
Tiagabine Hydrochloride 12 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-8072
Product details
- Brand name
- Tiagabine Hydrochloride
- Generic name
- Tiagabine Hydrochloride
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- NDA AUTHORIZED GENERIC · NDA020646
- Marketed since
- March 9, 2018
- Marketing end
- October 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Tiagabine Hydrochloride 12 mg/1
Uses, dosage, side effects and warnings for Tiagabine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-8072-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-8072-56) | Mar 9, 2018 |
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