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Diltiazem Hydrochloride

NDC 68682-371 · Oceanside Pharmaceuticals

Generic namediltiazem hydrochloride
Dosage formCAPSULE, EXTENDED RELEASE
RouteORAL
Active ingredient(s)DILTIAZEM HYDROCHLORIDE
Strength360 mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
Marketing categoryNDA AUTHORIZED GENERIC

Packages

68682-371-90 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68682-371-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

68462-850 — Diltiazem Hydrochloride, 68462-851 — Diltiazem Hydrochloride, 68682-006 — Diltiazem hydrochloride, 68682-007 — Diltiazem Hydrochloride, 68682-008 — Diltiazem Hydrochloride, 68682-009 — Diltiazem Hydrochloride, 68682-367 — diltiazem hydrochloride, 68682-368 — diltiazem hydrochloride, 68682-369 — diltiazem hydrochloride, 68682-370 — diltiazem hydrochloride, 68682-372 — diltiazem hydrochloride, 68682-704 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-705 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-706 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-707 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-708 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-709 — Diltiazem Hydrochloride Extended-Release Tablets, 68682-993 — Diltiazem hydrochloride, 68682-994 — Diltiazem Hydrochloride, 68682-997 — 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