Gabapentin 72189-0178
Product NDC
72189-0178- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 8, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA205101
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Gabapentin | 800 mg/1 |
Drug Class
Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(3)
30 TABLET in 1 BOTTLE (72189-178-30)
120 TABLET in 1 BOTTLE (72189-178-72)
90 TABLET in 1 BOTTLE (72189-178-90)