NDC 60687-583 – Carbamazepine

Carbamazepine 200 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC60687-583

Product details

Brand name
Carbamazepine
Generic name
Carbamazepine
Labeler
American Health Packaging
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA211623
Marketed since
January 5, 2022
Listing expires
December 31, 2027
Pharmacologic class
Mood Stabilizer

Active ingredients

Uses, dosage, side effects and warnings for Carbamazepine →

Package NDC codes (1)

Package NDCDescriptionSince
60687-583-2130 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-583-21) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (60687-583-11)Jan 5, 2022

Recalls mentioning this NDC

Other Carbamazepine products