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Edex
Edex - 52244-020-02 - (alprostadil)
Drug Information of Edex
| Product NDC: | 52244-020 |
| Proprietary Name: | Edex |
| Non Proprietary Name: | alprostadil |
| Active Ingredient(s): | 20 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: | 52244-020 |
| Labeler Name: | Actient Pharmaceuticals, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA020649 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20120115 |
Package Information of Edex
| Package NDC: | 52244-020-02 |
| Package Description: | 2 BLISTER PACK in 1 CARTON (52244-020-02) > 1 CARTRIDGE in 1 BLISTER PACK > 1 mL in 1 CARTRIDGE |
NDC Information of Edex
| NDC Code | 52244-020-02 |
| Proprietary Name | Edex |
| Package Description | 2 BLISTER PACK in 1 CARTON (52244-020-02) > 1 CARTRIDGE in 1 BLISTER PACK > 1 mL in 1 CARTRIDGE |
| Product NDC | 52244-020 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | alprostadil |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRACAVERNOUS |
| Start Marketing Date | 20120115 |
| Marketing Category Name | NDA |
| Labeler Name | Actient Pharmaceuticals, LLC |
| Substance Name | ALPROSTADIL |
| Strength Number | 20 |
| 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] |
