Product NDC: | 0517-2340 |
Proprietary Name: | Venofer |
Non Proprietary Name: | iron sucrose |
Active Ingredient(s): | 20 mg/mL & nbsp; iron sucrose |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-2340 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021135 |
Marketing Category: | NDA |
Start Marketing Date: | 20001110 |
Package NDC: | 0517-2340-10 |
Package Description: | 10 VIAL, SINGLE-USE in 1 TRAY (0517-2340-10) > 5 mL in 1 VIAL, SINGLE-USE |
NDC Code | 0517-2340-10 |
Proprietary Name | Venofer |
Package Description | 10 VIAL, SINGLE-USE in 1 TRAY (0517-2340-10) > 5 mL in 1 VIAL, SINGLE-USE |
Product NDC | 0517-2340 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | iron sucrose |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 20001110 |
Marketing Category Name | NDA |
Labeler Name | American Regent, Inc. |
Substance Name | IRON SUCROSE |
Strength Number | 20 |
Strength Unit | mg/mL |
Pharmaceutical Classes |