Edex - 52244-010-02 - (alprostadil)

Alphabetical Index


Drug Information of Edex

Product NDC: 52244-010
Proprietary Name: Edex
Non Proprietary Name: alprostadil
Active Ingredient(s): 10    ug/mL & nbsp;   alprostadil
Administration Route(s): INTRACAVERNOUS
Dosage Form(s): INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Edex

Product NDC: 52244-010
Labeler Name: Actient Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020649
Marketing Category: NDA
Start Marketing Date: 20120415

Package Information of Edex

Package NDC: 52244-010-02
Package Description: 2 BLISTER PACK in 1 CARTON (52244-010-02) > 1 CARTRIDGE in 1 BLISTER PACK > 1 mL in 1 CARTRIDGE

NDC Information of Edex

NDC Code 52244-010-02
Proprietary Name Edex
Package Description 2 BLISTER PACK in 1 CARTON (52244-010-02) > 1 CARTRIDGE in 1 BLISTER PACK > 1 mL in 1 CARTRIDGE
Product NDC 52244-010
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name alprostadil
Dosage Form Name INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route Name INTRACAVERNOUS
Start Marketing Date 20120415
Marketing Category Name NDA
Labeler Name Actient Pharmaceuticals, LLC
Substance Name ALPROSTADIL
Strength Number 10
Strength Unit ug/mL
Pharmaceutical Classes Genitourinary Arterial Vasodilation [PE],Prostaglandin Analog [EPC],Prostaglandin E1 Agonist [EPC],Prostaglandin Receptor Agonists [MoA],Prostaglandins [Chemical/Ingredient],Venous Vasodilation [PE]

Complete Information of Edex


General Information