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
- 0615-8380_72f92a1f-d8d6-494e-a8e9-875ca4bf4b50
- Product NDC
- 0615-8380
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- diltiazem hydrochloride
- Labeler
- NCS HealthCare of KY, LLC dba Vangard Labs
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190614
- Source listing expiry
- 20261231
Source-listed ingredients
- DILTIAZEM HYDROCHLORIDE — 180 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (0615-8380-39) · 0615-8380-39
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →