NDC 71335-3135 – Diltiazem Hydrochloride

Diltiazem Hydrochloride 90 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC71335-3135

Product details

Brand name
Diltiazem Hydrochloride
Generic name
Diltiazem Hydrochloride
Labeler
Bryant Ranch Prepack
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA216521
Marketed since
September 26, 2022
Listing expires
December 31, 2027
Pharmacologic class
Calcium Channel Blocker

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
71335-3135-130 TABLET in 1 BOTTLE (71335-3135-1)May 27, 2026
71335-3135-290 TABLET in 1 BOTTLE (71335-3135-2)May 27, 2026

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