Gabapentin 80425-0097
Product NDC
80425-0097- Manufacturer
- Advanced Rx Of Tennessee, Llc
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 6, 2011
- Listing Expires
- December 31, 2026
- 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(4)
30 TABLET, FILM COATED in 1 BOTTLE (80425-0097-1)
60 TABLET, FILM COATED in 1 BOTTLE (80425-0097-2)
90 TABLET, FILM COATED in 1 BOTTLE (80425-0097-3)
120 TABLET, FILM COATED in 1 BOTTLE (80425-0097-4)