NDC 52244-020 – Edex

Alprostadil 20 ug/mL · Injection, Powder, Lyophilized, For Solution · Intracavernous

Human Prescription Drug 1 recall

Product NDC52244-020

Product details

Brand name
Edex
Generic name
Alprostadil
Labeler
Endo USA, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intracavernous
Marketing category
NDA · NDA020649
Marketed since
January 15, 2012
Listing expires
December 31, 2027
Pharmacologic class
Prostaglandin Analog; Prostaglandin E1 Agonist

Active ingredients

Uses, dosage, side effects and warnings for Edex →

Package NDC codes (2)

Package NDCDescriptionSince
52244-020-022 BLISTER PACK in 1 CARTON (52244-020-02) / 1 CARTRIDGE in 1 BLISTER PACK / 1 mL in 1 CARTRIDGEJan 15, 2012
52244-020-066 BLISTER PACK in 1 CARTON (52244-020-06) / 1 CARTRIDGE in 1 BLISTER PACK / 1 mL in 1 CARTRIDGEJan 15, 2012

Recalls mentioning this NDC

Other Edex products