Gabapentin 68462-0127
Product NDC
68462-0127- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 1, 2006
- Listing Expires
- December 31, 2026
- Application
- ANDA077662
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 800 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
100 TABLET in 1 BOTTLE (68462-127-01)
500 TABLET in 1 BOTTLE (68462-127-05)