NDC 51407-215 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC51407-215

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
Golden State Medical Supply, 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 (2)

Package NDCDescriptionSince
51407-215-01100 TABLET in 1 BOTTLE (51407-215-01)May 9, 2019
51407-215-101000 TABLET in 1 BOTTLE (51407-215-10)May 9, 2019

Recalls mentioning this NDC

Other Carbamazepine products