Gabapentin 70518-2912
Product NDC
70518-2912- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 20, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA206402
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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)
100 POUCH in 1 BOX (70518-2912-2) / 1 TABLET in 1 POUCH (70518-2912-3)