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
- 47335-678_3c94f868-93d3-4b36-8420-b2903a0bd79a
- Product NDC
- 47335-678
- Form
- CAPSULE, EXTENDED RELEASE
- Composition / generic term
- Diltiazem Hydrochloride
- Labeler
- Sun Pharmaceutical Industries, Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111031
- Source listing expiry
- 20261231
Source-listed ingredients
- DILTIAZEM HYDROCHLORIDE — 300 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-13) · 47335-678-13
- 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-18) · 47335-678-18
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-19) · 47335-678-19
- 90 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-81) · 47335-678-81
- 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-678-83) · 47335-678-83
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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