# Edex

NDC: 52244-040
Generic name: alprostadil
Labeler / Manufacturer: Endo USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRACAVERNOUS
Marketing started: 20120315

FDA application: NDA020649

## Active ingredients

- ALPROSTADIL: 40 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52244-040"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52244-040
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e8b8ec8d-1318-43e4-a182-446e9f9579de