NDC 0093-5030 – Tiagabine Hydrochloride
Tiagabine Hydrochloride 2 mg/1 · Tablet, Film Coated · Oral
Product NDC0093-5030
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
- June 3, 2016
- Marketing end
- October 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Tiagabine Hydrochloride 2 mg/1
Uses, dosage, side effects and warnings for Tiagabine Hydrochloride →
Package NDC codes (1)
| Package NDC | Description | Since |
|---|---|---|
| 0093-5030-56 | 30 TABLET, FILM COATED in 1 BOTTLE (0093-5030-56) | Jun 3, 2016 |
Other Tiagabine Hydrochloride products
- 62756-200 Tiagabine Hydrochloride 2 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 62756-224 Tiagabine Hydrochloride 4 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
- 0093-5031 Tiagabine Hydrochloride 4 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.
- 0093-8072 Tiagabine Hydrochloride 12 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.
- 0093-8076 Tiagabine Hydrochloride 16 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.
- 72205-084 Tiagabine Hydrochloride 2 mg/1 · Tablet · Novadoz Pharmaceuticals LLC
- 72205-085 Tiagabine Hydrochloride 4 mg/1 · Tablet · Novadoz Pharmaceuticals LLC
- 72205-086 Tiagabine Hydrochloride 12 mg/1 · Tablet · Novadoz Pharmaceuticals LLC
- 72205-087 Tiagabine Hydrochloride 16 mg/1 · Tablet · Novadoz Pharmaceuticals LLC