NDC 47335-679 – Diltiazem Hydrochloride

Diltiazem Hydrochloride 360 mg/1 · Capsule, Extended Release · Oral

Human Prescription Drug 1 recall

Product NDC47335-679

Product details

Brand name
Diltiazem Hydrochloride
Generic name
Diltiazem Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Capsule, Extended Release
Route
Oral
Marketing category
ANDA · ANDA090492
Marketed since
October 31, 2011
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker

Active ingredients

Uses, dosage, side effects and warnings for Diltiazem Hydrochloride →

Package NDC codes (5)

Package NDCDescriptionSince
47335-679-13500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-13)Oct 31, 2011
47335-679-181000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-18)Oct 31, 2011
47335-679-1990 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-19)Oct 31, 2011
47335-679-8190 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-81)Oct 31, 2011
47335-679-8330 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-679-83)Oct 31, 2011

Recalls mentioning this NDC

Other Diltiazem Hydrochloride products