NDC 51991-293 – Oxcarbazepine

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

Human Prescription Drug

Product NDC51991-293

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Breckenridge Pharmaceutical, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA078069
Marketed since
January 11, 2008
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (2)

Package NDCDescriptionSince
51991-293-01100 TABLET, FILM COATED in 1 BOTTLE (51991-293-01)Jan 11, 2008
51991-293-05500 TABLET, FILM COATED in 1 BOTTLE (51991-293-05)Jan 11, 2008

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