Gabapentin 68071-2214
Product NDC
68071-2214- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 4, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205101
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 800 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(1)
90 TABLET in 1 BOTTLE (68071-2214-9)