NDC 0078-0457 – Trileptal

Oxcarbazepine 600 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0078-0457

Product details

Brand name
Trileptal
Generic name
Oxcarbazepine
Labeler
Novartis Pharmaceuticals Corporation
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
NDA · NDA021014
Marketed since
January 30, 2000
Listing expires
December 31, 2026
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Trileptal →

Package NDC codes (2)

Package NDCDescriptionSince
0078-0457-05100 TABLET, FILM COATED in 1 BOTTLE (0078-0457-05)Jan 30, 2000
0078-0457-35100 BLISTER PACK in 1 BOX, UNIT-DOSE (0078-0457-35) / 1 TABLET, FILM COATED in 1 BLISTER PACK (0078-0457-61)Jan 30, 2000

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