United States · FDA National Drug Code directory

Diltiazem Hydrochloride

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference: 46708-781_74bab197-f719-48c0-ac84-c0cf0087b45a
Product NDC: 46708-781
Form: TABLET, FILM COATED
Composition / generic term: Diltiazem Hydrochloride
Labeler: Alembic Pharmaceuticals Limited
Marketing category: ANDA
Marketing start / end (source format): 20251114
Source listing expiry: 20261231

Source-listed ingredients

DILTIAZEM HYDROCHLORIDE — 30 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

100 TABLET, FILM COATED in 1 BOTTLE (46708-781-31) · 46708-781-31
500 TABLET, FILM COATED in 1 BOTTLE (46708-781-71) · 46708-781-71

Source and coverage

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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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