Gabapentin 65841-0705
Product NDC
65841-0705- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 16, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA078926
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 600 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (65841-705-01)
500 TABLET, FILM COATED in 1 BOTTLE (65841-705-05)
1000 TABLET, FILM COATED in 1 BOTTLE (65841-705-10)