NDC 62756-224 – Tiagabine Hydrochloride
Tiagabine Hydrochloride 4 mg/1 · Tablet, Film Coated · Oral
Product NDC62756-224
Product details
- Brand name
- Tiagabine Hydrochloride
- Generic name
- Tiagabine Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077555
- Marketed since
- November 4, 2011
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anti-epileptic Agent
Active ingredients
- Tiagabine Hydrochloride 4 mg/1
Uses, dosage, side effects and warnings for Tiagabine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 62756-224-08 | 100 TABLET, FILM COATED in 1 BOTTLE (62756-224-08) | Nov 4, 2011 |
| 62756-224-18 | 1000 TABLET, FILM COATED in 1 BOTTLE (62756-224-18) | Nov 4, 2011 |
| 62756-224-83 | 30 TABLET, FILM COATED in 1 BOTTLE (62756-224-83) | Nov 4, 2011 |
| 62756-224-88 | 100 TABLET, FILM COATED in 1 BOTTLE (62756-224-88) | Nov 4, 2011 |
Recalls mentioning this NDC
- D-0914-2023 Jul 19, 2023 · Class II
Failed Impurities: Out of Specification (OOS) result observed during Related Substances testing
Other Tiagabine Hydrochloride products
- 62756-200 Tiagabine Hydrochloride 2 mg/1 · Tablet, Film Coated · Sun Pharmaceutical Industries, Inc.
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- 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