Oxcarbazepine 60687-0733
Product NDC
60687-0733- Manufacturer
- American Health Packaging
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 27, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA215939
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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(1)
100 BLISTER PACK in 1 CARTON (60687-733-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-733-11)