United States · FDA National Drug Code directory

Diltiazem Hydrochloride EXTENDED RELEASE

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: 71335-1585_9308bc71-ce3f-429f-9926-d140481ad8ab
Product NDC: 71335-1585
Form: CAPSULE, EXTENDED RELEASE
Composition / generic term: diltiazem hydrochloride
Labeler: Bryant Ranch Prepack
Marketing category: NDA AUTHORIZED GENERIC
Marketing start / end (source format): 20140820
Source listing expiry: 20261231

Source-listed ingredients

DILTIAZEM HYDROCHLORIDE — 240 mg/1

These values do not establish equivalence or a dose recommendation.

Packages

30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-1) · 71335-1585-1
90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-2) · 71335-1585-2
18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-1585-3) · 71335-1585-3

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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