Gabapentin 70771-1862
Product NDC
70771-1862- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 25, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA203934
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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)
10 BLISTER PACK in 1 CARTON (70771-1862-4) / 10 TABLET in 1 BLISTER PACK (70771-1862-2)
500 TABLET in 1 BOTTLE (70771-1862-5)
90 TABLET in 1 BOTTLE (70771-1862-9)