Tiagabine Hydrochloride 72205-0084
Product NDC
72205-0084- Manufacturer
- Novadoz Pharmaceuticals Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 23, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA214816
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tiagabine Hydrochloride | 2 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(1)
30 TABLET in 1 BOTTLE (72205-084-30)