Gabapentin 68382-0357
Product NDC
68382-0357- Manufacturer
- Zydus Pharmaceuticals Usa Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 18, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA203934
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 900 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
100 TABLET in 1 BOTTLE (68382-357-01)
60 TABLET in 1 BOTTLE (68382-357-14)