United States · FDA National Drug Code directory
INFUMORPH 200
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
- 0641-6039_b1c060cb-5c5b-495f-90b5-044e04f2a3f2
- Product NDC
- 0641-6039
- Form
- INJECTION, SOLUTION
- 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 — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 mL in 1 AMPULE (0641-6039-01) · 0641-6039-01
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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