NDC 72189-339 – Oxcarbazepine

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

Human Prescription Drug

Product NDC72189-339

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
DirectRx
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077794
Marketed since
April 5, 2022
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
72189-339-6060 TABLET, FILM COATED in 1 BOTTLE (72189-339-60)Apr 5, 2022

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