NDC 0093-0321 – Diltiazem Hydrochloride

Diltiazem Hydrochloride 120 mg/1 · Tablet, Film Coated · Oral

Human Prescription Drug

Product NDC0093-0321

Product details

Brand name
Diltiazem Hydrochloride
Generic name
Diltiazem Hydrochloride
Labeler
Teva Pharmaceuticals USA, Inc.
Dosage form
Tablet, Film Coated
Route
Oral
Marketing category
ANDA · ANDA074185
Marketed since
December 26, 1995
Listing expires
December 31, 2026
Pharmacologic class
Calcium Channel Blocker

Active ingredients

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

Package NDC codes (1)

Package NDCDescriptionSince
0093-0321-01100 TABLET, FILM COATED in 1 BOTTLE (0093-0321-01)Dec 26, 1995

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