NDC 62559-220 – Oxcarbazepine

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

Human Prescription Drug

Product NDC62559-220

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
ANI Pharmaceuticals, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078005
Marketed since
July 15, 2025
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (2)

Package NDCDescriptionSince
62559-220-01100 TABLET, FILM COATED in 1 BOTTLE (62559-220-01)Jul 15, 2025
62559-220-05500 TABLET, FILM COATED in 1 BOTTLE (62559-220-05)Jul 15, 2025

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