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
- 50742-565_3dd3b71c-60fb-45a2-866e-7761f1c48aa3
- Product NDC
- 50742-565
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- diltiazem hydrochloride
- Labeler
- Ingenus Pharmaceuticals, LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20250703
- Source listing expiry
- 20261231
Source-listed ingredients
- DILTIAZEM HYDROCHLORIDE — 90 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-565-01) · 50742-565-01
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50742-565-05) · 50742-565-05
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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