Oxcarbazepine 68462-0139
Product NDC
68462-0139- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- October 9, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077802
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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 (68462-139-01)
500 TABLET, FILM COATED in 1 BOTTLE (68462-139-05)