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Caverject Impulse
Caverject Impulse - 0009-5182-01 - (Alprostadil)
Drug Information of Caverject Impulse
| Product NDC: | 0009-5182 |
| Proprietary Name: | Caverject Impulse |
| Non Proprietary Name: | Alprostadil |
| Active Ingredient(s): | 20 ug/.5mL & nbsp; Alprostadil |
| Administration Route(s): | INTRACAVERNOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Caverject Impulse
| Product NDC: | 0009-5182 |
| Labeler Name: | Pharmacia and Upjohn Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA021212 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20020611 |
Package Information of Caverject Impulse
| Package NDC: | 0009-5182-01 |
| Package Description: | 2 SYRINGE in 1 CARTON (0009-5182-01) > .5 mL in 1 SYRINGE |
NDC Information of Caverject Impulse
| NDC Code | 0009-5182-01 |
| Proprietary Name | Caverject Impulse |
| Package Description | 2 SYRINGE in 1 CARTON (0009-5182-01) > .5 mL in 1 SYRINGE |
| Product NDC | 0009-5182 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Alprostadil |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRACAVERNOUS |
| Start Marketing Date | 20020611 |
| Marketing Category Name | NDA |
| Labeler Name | Pharmacia and Upjohn Company |
| Substance Name | ALPROSTADIL |
| Strength Number | 20 |
| Strength Unit | ug/.5mL |
| Pharmaceutical Classes | Genitourinary Arterial Vasodilation [PE],Prostaglandin Analog [EPC],Prostaglandin E1 Agonist [EPC],Prostaglandin Receptor Agonists [MoA],Prostaglandins [Chemical/Ingredient],Venous Vasodilation [PE] |
