Product NDC: | 65847-205 |
Proprietary Name: | NATRECOR |
Non Proprietary Name: | NESIRITIDE |
Active Ingredient(s): | 1.5 mg/5mL & nbsp; NESIRITIDE |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 65847-205 |
Labeler Name: | Scios Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020920 |
Marketing Category: | NDA |
Start Marketing Date: | 20010801 |
Package NDC: | 65847-205-25 |
Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (65847-205-25) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Code | 65847-205-25 |
Proprietary Name | NATRECOR |
Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (65847-205-25) > 5 mL in 1 VIAL, SINGLE-USE |
Product NDC | 65847-205 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | NESIRITIDE |
Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20010801 |
Marketing Category Name | NDA |
Labeler Name | Scios Inc. |
Substance Name | NESIRITIDE |
Strength Number | 1.5 |
Strength Unit | mg/5mL |
Pharmaceutical Classes | Natriuretic Peptide [EPC],Natriuretic Peptides [Chemical/Ingredient] |