# Duramorph

NDC: 0641-6020
Generic name: morphine sulfate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: EPIDURAL, INTRATHECAL, INTRAVENOUS
Marketing started: 19840918

FDA application: NDA018565

## Active ingredients

- MORPHINE SULFATE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0641-6020"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6020
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ebb18761-e5c4-4238-bb84-f9549f500210