NDC 62037-599 – Cartia XT

Diltiazem Hydrochloride 240 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC62037-599

Product details

Brand name
Cartia XT
Generic name
Diltiazem Hydrochloride
Labeler
Actavis Pharma, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA074752
Marketed since
July 9, 1998
Listing expires
December 31, 2027
Pharmacologic class
Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Cartia →

Package NDC codes (2)

Package NDCDescriptionSince
62037-599-05500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-599-05)Jun 23, 1999
62037-599-9090 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (62037-599-90)Jun 23, 1999

Recalls mentioning this NDC

Other Cartia products