NDC 67046-2084 – Oxcarbazepine

Oxcarbazepine 300 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC67046-2084

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Coupler LLC
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215939
Marketed since
May 6, 2026
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for oxcarbazepine →

Package NDC codes (1)

Package NDCDescriptionSince
67046-2084-330 TABLET, FILM COATED in 1 BLISTER PACK (67046-2084-3)May 6, 2026

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