NDC 62756-185 – Oxcarbazepine

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

Human Prescription Drug 2 recalls

Product NDC62756-185

Product details

Brand name
Oxcarbazepine
Generic name
Oxcarbazepine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA077794
Marketed since
October 9, 2007
Listing expires
December 31, 2027
Pharmacologic class
Anti-epileptic Agent

Active ingredients

Uses, dosage, side effects and warnings for Oxcarbazepine →

Package NDC codes (5)

Package NDCDescriptionSince
62756-185-08100 TABLET, FILM COATED in 1 BOTTLE (62756-185-08)Oct 9, 2007
62756-185-13500 TABLET, FILM COATED in 1 BOTTLE (62756-185-13)Oct 9, 2007
62756-185-181000 TABLET, FILM COATED in 1 BOTTLE (62756-185-18)Oct 9, 2007
62756-185-8330 TABLET, FILM COATED in 1 BOTTLE (62756-185-83)Oct 9, 2007
62756-185-88100 TABLET, FILM COATED in 1 BOTTLE (62756-185-88)Oct 9, 2007

Recalls mentioning this NDC

Other Oxcarbazepine products