Oxcarbazepine 51672-1393-01

Package NDC

51672-1393-01

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]

Selected Package

51672-1393-01Selected

1 BOTTLE, GLASS in 1 CARTON (51672-1393-1) / 250 mL in 1 BOTTLE, GLASS