Oxcarbazepine 68462-0137
Product NDC
68462-0137- 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
Need to source Oxcarbazepine? Find it on a pharmacy-to-pharmacy marketplace at better prices.
✓ DSCSA Compliant. ✓ Verified Pharmacies Only.P2P pharmacy marketplace.
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)
100 TABLET, FILM COATED in 1 BOTTLE (68462-137-01)
500 TABLET, FILM COATED in 1 BOTTLE (68462-137-05)