NDC 87063-208 – Oxcarbazepine

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

Human Prescription Drug

Product NDC87063-208

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
ASCLEMED USA INC.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA215939
Marketed since
January 11, 2022
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (4)

Package NDCDescriptionSince
87063-208-01100 TABLET, FILM COATED in 1 BOTTLE (87063-208-01)May 19, 2026
87063-208-3030 TABLET, FILM COATED in 1 BOTTLE (87063-208-30)May 19, 2026
87063-208-6060 TABLET, FILM COATED in 1 BOTTLE (87063-208-60)May 19, 2026
87063-208-9090 TABLET, FILM COATED in 1 BOTTLE (87063-208-90)May 19, 2026

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