NDC 71335-0579 – Diltiazem Hydrochloride

Diltiazem Hydrochloride 90 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-0579

Product details

Brand name
Diltiazem Hydrochloride
Generic name
Diltiazem Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA018602
Marketed since
December 25, 2010
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71335-0579-130 TABLET in 1 BOTTLE (71335-0579-1)Dec 27, 2021
71335-0579-290 TABLET in 1 BOTTLE (71335-0579-2)Mar 13, 2018

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