Gabapentin 16571-0117
Product NDC
16571-0117- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 19, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA217995
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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 (16571-117-01)
500 TABLET in 1 BOTTLE (16571-117-50)