Gabapentin 72789-0217
Product NDC
72789-0217- Manufacturer
- Pd-Rx Pharmaceuticals, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- February 4, 2016
- 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(1)
60 TABLET in 1 BOTTLE, PLASTIC (72789-217-60)