NDC 50742-611 – Oxcarbazepine

Oxcarbazepine 150 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC50742-611

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Ingenus Pharmaceuticals, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA215796
Marketed since
June 1, 2025
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (1)

Package NDCDescriptionSince
50742-611-01100 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-611-01)Jun 1, 2025

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