United States · FDA National Drug Code directory
Edex
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
- 52244-040_160196d5-a339-455d-8b68-4c9f437929a5
- Product NDC
- 52244-040
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- alprostadil
- Labeler
- Endo USA, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20120315
- Source listing expiry
- 20271231
Source-listed ingredients
- ALPROSTADIL — 40 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 2 BLISTER PACK in 1 CARTON (52244-040-02) / 1 CARTRIDGE in 1 BLISTER PACK / 1 mL in 1 CARTRIDGE · 52244-040-02
- 6 BLISTER PACK in 1 CARTON (52244-040-06) / 1 CARTRIDGE in 1 BLISTER PACK / 1 mL in 1 CARTRIDGE · 52244-040-06
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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