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
- 71335-3091_8cef16b7-12fc-4ff4-8379-ec6c9a4b2a19
- Product NDC
- 71335-3091
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- diltiazem hydrochloride
- Labeler
- Bryant Ranch Prepack
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190614
- Source listing expiry
- 20271231
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 (71335-3091-1) · 71335-3091-1
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-3091-2) · 71335-3091-2
- 18 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-3091-3) · 71335-3091-3
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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