Tiagabine Hydrochloride 12 mg / 1 Tablet 30 Tablet, Film Coated
Comprehensive product details for sourcing and verification.
| NDC 11 | 00093-8072-56 |
|---|---|
| Product NDC | 00093-8072 |
| Generic Drug Name | Tiagabine Hydrochloride |
| Brand Name | Tiagabine Hydrochloride |
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
| Strength | 12 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0093-8072-56) |
| Active Ingredients | Tiagabine Hydrochloride |
| Marketing Category | NDA AUTHORIZED GENERIC |
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NDC snapshot
Tiagabine Hydrochloride 12 mg / 1 Tablet is tracked under NDC 00093-8072-56 and rolls up into product family 00093-8072. Use this page to confirm the exact presentation before moving into related family or manufacturer pathways.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Teva Pharmaceuticals USA, Inc..
- Dosage form: Tablet.
- Family size: 1 active presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Tiagabine Hydrochloride 12 mg / 1 Tablet 30 Tablet, Film Coated, NDC 00093-8072-56, is a Teva Pharmaceuticals USA, Inc. 12 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 00093-8072-56.
- Digits-only NDC 11: 00093807256.
- Possible 10-digit display format: 0093-8072-56 (0093807256).
Helpful product links
- Search by brand name: Tiagabine Hydrochloride.
- Exact NDC 11: 00093-8072-56.
- Product family NDC: 00093-8072.