NDC 0904-7594 – Oxcarbazepine

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

Human Prescription Drug

Product NDC0904-7594

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Major Pharmaceuticals
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078069
Marketed since
April 3, 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
0904-7594-61100 BLISTER PACK in 1 CARTON (0904-7594-61) / 1 TABLET, FILM COATED in 1 BLISTER PACKApr 3, 2026

Other Oxcarbazepine products