Gabapentin 70518-2323
Product NDC
70518-2323- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 24, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA200651
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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)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2323-0)
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-1)
120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2323-3)
100 POUCH in 1 BOX (70518-2323-4) / 1 TABLET, FILM COATED in 1 POUCH (70518-2323-5)