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Diltiazem Hydrochloride

NDC 46708-782 · Alembic Pharmaceuticals Limited

Generic nameDiltiazem Hydrochloride
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)DILTIAZEM HYDROCHLORIDE
Strength60 mg/1
Pharmacologic classCalcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA]
Marketing categoryANDA

Packages

46708-782-31 — 100 TABLET, FILM COATED in 1 BOTTLE (46708-782-31)

46708-782-71 — 500 TABLET, FILM COATED in 1 BOTTLE (46708-782-71)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

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, 46708-781 — Diltiazem Hydrochloride, 46708-783 — Diltiazem Hydrochloride, 46708-784 — Diltiazem Hydrochloride, 46708-815 — Diltiazem Hydrochloride, 46708-816 — Diltiazem Hydrochloride, 46708-817 — Diltiazem Hydrochloride, 47335-669 — Diltiazem Hydrochloride, 47335-670 — Diltiazem Hydrochloride, 47335-671 — Diltiazem Hydrochloride, 47335-672 — Diltiazem Hydrochloride, 47335-673 — 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.