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Diltiazem hydrochloride

NDC 63304-719 · Sun Pharmaceutical Industries, Inc.

Generic nameDiltiazem hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)DILTIAZEM HYDROCHLORIDE
Strength180 mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
Marketing categoryANDA

Packages

63304-719-05 — 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-719-05)

63304-719-30 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-719-30)

63304-719-90 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (63304-719-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

62332-729 — Diltiazem Hydrochloride, 62332-781 — Diltiazem Hydrochloride, 62332-782 — Diltiazem Hydrochloride, 62332-783 — 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, 63304-720 — Diltiazem hydrochloride, 63304-721 — Diltiazem hydrochloride, 63304-722 — Diltiazem hydrochloride, 63629-2154 — Diltiazem Hydrochloride, 63629-2158 — Diltiazem Hydrochloride, 63629-2159 — Diltiazem Hydrochloride, 63629-3659 — Diltiazem Hydrochloride, 63629-7896 — Diltiazem Hydrochloride, 63629-7981 — diltiazem hydrochloride, 67046-1481 — 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.

Read from: FDA National Drug Code Directory, product.txt and package.txt (accessdata.fda.gov/cder/ndctext.zip) — Snapshot retrieved 2026-08-24, loaded 2026-08-24; CMS Medicare Part B Drug Average Sales Price (ASP) Pricing Files (cms.gov/medicare/payment/part-b-drugs/asp-pricing-files) -- the NDC-HCPCS crosswalk and Part B payment limit files — 2026 Q3 (July 2026 release). All data sources · How to read the labels