Oxcarbazepine 62559-0222
Product NDC
62559-0222- Manufacturer
- Ani Pharmaceuticals, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 15, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA078005
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxcarbazepine | 600 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (62559-222-01)
500 TABLET, FILM COATED in 1 BOTTLE (62559-222-05)