United States · FDA National Drug Code directory
Duramorph
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
- 0641-6019_aa74af85-7068-4254-9a79-c7f3792044a6
- Product NDC
- 0641-6019
- Form
- INJECTION
- Composition / generic term
- morphine sulfate
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 19840918
- Source listing expiry
- 20271231
Source-listed ingredients
- MORPHINE SULFATE — 1 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 10 AMPULE in 1 CARTON (0641-6019-10) / 10 mL in 1 AMPULE (0641-6019-01) · 0641-6019-10
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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