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Diltiazem Hydrochloride

NDC 33342-522 · Macleods Pharmaceuticals Limited

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

33342-522-02 — 6 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (33342-522-02)

33342-522-07 — 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-522-07)

33342-522-10 — 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (33342-522-10)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

24979-026 — Diltiazem hydrochloride, 24979-027 — Diltiazem hydrochloride, 24979-028 — Diltiazem hydrochloride, 24979-029 — Diltiazem hydrochloride, 24979-030 — Diltiazem hydrochloride, 24979-181 — diltiazem hydrochloride, 24979-182 — diltiazem hydrochloride, 24979-183 — diltiazem hydrochloride, 25021-319 — diltiazem hydrochloride, 33342-521 — Diltiazem Hydrochloride, 33342-523 — Diltiazem Hydrochloride, 33342-524 — Diltiazem Hydrochloride, 33342-525 — Diltiazem Hydrochloride, 44567-662 — Diltiazem Hydrochloride, 44567-663 — Diltiazem Hydrochloride, 46708-725 — Diltiazem Hydrochloride, 46708-726 — Diltiazem Hydrochloride, 46708-727 — Diltiazem Hydrochloride, 46708-728 — Diltiazem Hydrochloride, 46708-729 — 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.