NDC 0904-6172 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC0904-6172

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Major Pharmaceuticals
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077272
Marketed since
September 20, 2010
Listing expires
December 31, 2027
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Carbamazepine →

Package NDC codes (2)

Package NDCDescriptionSince
0904-6172-502000 TABLET in 1 BOTTLE (0904-6172-50)Sep 20, 2010
0904-6172-61100 BLISTER PACK in 1 CARTON (0904-6172-61) / 1 TABLET in 1 BLISTER PACKSep 20, 2010

Recalls mentioning this NDC

Other Carbamazepine products