Gabapentin 70518-2356
Product NDC
70518-2356- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 9, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA200651
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 600 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2356-0)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2356-1)