NDC 72205-084 – Tiagabine Hydrochloride
Tiagabine Hydrochloride 2 mg/1 · Tablet · Oral
Product NDC72205-084
Product details
- Brand name
- Tiagabine Hydrochloride
- Generic name
- Tiagabine Hydrochloride
- Labeler
- Novadoz Pharmaceuticals LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA214816
- Marketed since
- November 23, 2021
- Listing expires
- December 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 |
|---|---|---|
| 72205-084-30 | 30 TABLET in 1 BOTTLE (72205-084-30) | Nov 23, 2021 |
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- 0093-8076 Tiagabine Hydrochloride 16 mg/1 · Tablet, Film Coated · Teva Pharmaceuticals USA, Inc.