NDC 70771-1932 – Diltiazem hydrochloride

Diltiazem Hydrochloride 120 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC70771-1932

Product details

Brand name
Diltiazem hydrochloride
Generic name
Diltiazem hydrochloride
Labeler
Zydus Lifesciences Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA219253
Marketed since
May 25, 2026
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
70771-1932-1100 TABLET in 1 BOTTLE (70771-1932-1)May 25, 2026
70771-1932-5500 TABLET in 1 BOTTLE (70771-1932-5)May 25, 2026

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