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
- 71335-0009_ceaca8e0-d681-4458-9a5a-2eb9e770755c
- Product NDC
- 71335-0009
- Form
- CAPSULE, COATED, EXTENDED RELEASE
- Composition / generic term
- Diltiazem Hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20151001
- 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, COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0009-1) · 71335-0009-1
- 90 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0009-2) · 71335-0009-2
- 18 CAPSULE, COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0009-3) · 71335-0009-3
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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