Tiagabine Hydrochloride 12 mg / 1 Tablet 30 Tablet
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 72205-0086-30 |
|---|---|
| Product NDC | 72205-0086 |
| Generic Drug Name | Tiagabine Hydrochloride |
| Brand Name | Tiagabine Hydrochloride |
| Manufacturer | Novadoz Pharmaceuticals LLC |
| Strength | 12 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet |
| Package Description | 30 TABLET in 1 BOTTLE (72205-086-30) |
| Active Ingredients | Tiagabine Hydrochloride |
| Marketing Category | ANDA |
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NDC snapshot
Tiagabine Hydrochloride 12 mg / 1 Tablet is tracked under NDC 72205-0086-30 and rolls up into product family 72205-0086. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 30 Tablet.
- Manufacturer: Novadoz Pharmaceuticals LLC.
- Dosage form: Tablet.
- Family size: 1 indexed 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, NDC 72205-0086-30, is a Novadoz Pharmaceuticals LLC 12 mg / 1 tablet presentation packaged as 30 Tablet.
NDC search formats
- Canonical NDC 11: 72205-0086-30
- Digits-only NDC 11: 72205008630
- Possible 10-digit display format: 72205-086-30 (7220508630)
Helpful product links
- Search by brand name: Tiagabine Hydrochloride
- NDC 11: 72205-0086-30
- Product family NDC: 72205-0086
- VA classification code: CN400
- VA classification code description: ANTICONVULSANTS
- CMOP ID: T0392
- VUID: 4013149