NDC 51672-4005 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet · Oral

Human Prescription Drug 2 recalls

Product NDC51672-4005

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA074649
Marketed since
October 3, 1996
Listing expires
December 31, 2027
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Carbamazepine →

Package NDC codes (3)

Package NDCDescriptionSince
51672-4005-1100 TABLET in 1 BOTTLE (51672-4005-1)Oct 3, 1996
51672-4005-2500 TABLET in 1 BOTTLE (51672-4005-2)Oct 3, 1996
51672-4005-31000 TABLET in 1 BOTTLE (51672-4005-3)Oct 3, 1996

Recalls mentioning this NDC

Other Carbamazepine products