NDC 72189-573 – Oxcarbazepine

Oxcarbazepine 150 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC72189-573

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Direct_rx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077802
Marketed since
September 9, 2024
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
72189-573-6060 TABLET, FILM COATED in 1 BOTTLE (72189-573-60)Sep 9, 2024

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