Product NDC: | 0037-8120 |
Proprietary Name: | MUSE |
Non Proprietary Name: | Alprostadil |
Active Ingredient(s): | 250 ug/1 & nbsp; Alprostadil |
Administration Route(s): | URETHRAL |
Dosage Form(s): | SUPPOSITORY |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0037-8120 |
Labeler Name: | Meda Pharmaceuticals Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020700 |
Marketing Category: | NDA |
Start Marketing Date: | 20110722 |
Package NDC: | 0037-8120-01 |
Package Description: | 6 POUCH in 1 CARTON (0037-8120-01) > 1 SUPPOSITORY in 1 POUCH (0037-8120-06) |
NDC Code | 0037-8120-01 |
Proprietary Name | MUSE |
Package Description | 6 POUCH in 1 CARTON (0037-8120-01) > 1 SUPPOSITORY in 1 POUCH (0037-8120-06) |
Product NDC | 0037-8120 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Alprostadil |
Dosage Form Name | SUPPOSITORY |
Route Name | URETHRAL |
Start Marketing Date | 20110722 |
Marketing Category Name | NDA |
Labeler Name | Meda Pharmaceuticals Inc. |
Substance Name | ALPROSTADIL |
Strength Number | 250 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Genitourinary Arterial Vasodilation [PE],Prostaglandin Analog [EPC],Prostaglandin E1 Agonist [EPC],Prostaglandin Receptor Agonists [MoA],Prostaglandins [Chemical/Ingredient],Venous Vasodilation [PE] |