Oxcarbazepine 70518-3940
Product NDC
70518-3940- Manufacturer
- Remedyrepack Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- December 6, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA215939
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxcarbazepine | 150 mg/1 |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3940-0)
100 POUCH in 1 BOX (70518-3940-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-3940-2)