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Diltiazem Hydrochloride

NDC 62332-783 · Alembic Pharmaceuticals Inc.

Generic nameDiltiazem Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)DILTIAZEM HYDROCHLORIDE
Strength90 mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
Marketing categoryANDA

Packages

62332-783-31 — 100 TABLET, FILM COATED in 1 BOTTLE (62332-783-31)

62332-783-71 — 500 TABLET, FILM COATED in 1 BOTTLE (62332-783-71)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62135-334 — Diltiazem Hydrochloride, 62135-335 — Diltiazem Hydrochloride, 62135-336 — Diltiazem Hydrochloride, 62332-725 — Diltiazem Hydrochloride, 62332-726 — Diltiazem Hydrochloride, 62332-727 — Diltiazem Hydrochloride, 62332-728 — Diltiazem Hydrochloride, 62332-729 — Diltiazem Hydrochloride, 62332-781 — Diltiazem Hydrochloride, 62332-782 — Diltiazem Hydrochloride, 62332-784 — Diltiazem Hydrochloride, 62332-815 — Diltiazem Hydrochloride, 62332-816 — Diltiazem Hydrochloride, 62332-817 — Diltiazem Hydrochloride, 63187-769 — Diltiazem Hydrochloride, 63304-718 — Diltiazem hydrochloride, 63304-719 — Diltiazem hydrochloride, 63304-720 — Diltiazem hydrochloride, 63304-721 — Diltiazem hydrochloride, 63304-722 — Diltiazem hydrochloride, +275 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.