NDC 51672-4123 – Carbamazepine

Carbamazepine 100 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC51672-4123

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA078115
Marketed since
March 31, 2009
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
51672-4123-1100 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4123-1)Mar 31, 2009
51672-4123-31000 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4123-3)Mar 31, 2009
51672-4123-630 TABLET, EXTENDED RELEASE in 1 BOTTLE (51672-4123-6)Mar 31, 2009

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