Gabapentin 65841-0706
Product NDC
65841-0706- 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 | 800 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(4)
100 TABLET, FILM COATED in 1 BOTTLE (65841-706-01)
500 TABLET, FILM COATED in 1 BOTTLE (65841-706-05)
1000 TABLET, FILM COATED in 1 BOTTLE (65841-706-10)
10 BLISTER PACK in 1 CARTON (65841-706-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK