# Panhematin

NDC: 55292-702
Generic name: hemin
Labeler / Manufacturer: Recordati Rare Diseases, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: POWDER, FOR SOLUTION
Routes: INTRAVENOUS
Marketing started: 19830720

FDA application: BLA101246

## Active ingredients

- HEMIN: 7 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55292-702"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55292-702
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9984267a-4d57-4444-9bb5-16bca7dea691