Oxcarbazepine 51672-1393
Product NDC
51672-1393- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 6, 2025
- Listing Expires
- December 31, 2026
- Application
- ANDA078734
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Oxcarbazepine | 60 mg/mL |
Drug Class
Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Decreased Central Nervous System Disorganized Electrical Activity [PE]
Packaging Options(1)
1 BOTTLE, GLASS in 1 CARTON (51672-1393-1) / 250 mL in 1 BOTTLE, GLASS