Product NDC: | 0517-0134 |
Proprietary Name: | Dexferrum |
Non Proprietary Name: | iron dextran |
Active Ingredient(s): | 50 mg/mL & nbsp; iron dextran |
Administration Route(s): | INTRAVENOUS |
Dosage Form(s): | INJECTION, SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0517-0134 |
Labeler Name: | American Regent, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA040024 |
Marketing Category: | NDA |
Start Marketing Date: | 19981001 |
Package NDC: | 0517-0134-10 |
Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-0134-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0517-0134-10 |
Proprietary Name | Dexferrum |
Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-0134-10) > 1 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0517-0134 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | iron dextran |
Dosage Form Name | INJECTION, SOLUTION |
Route Name | INTRAVENOUS |
Start Marketing Date | 19981001 |
Marketing Category Name | NDA |
Labeler Name | American Regent, Inc. |
Substance Name | IRON DEXTRAN |
Strength Number | 50 |
Strength Unit | mg/mL |
Pharmaceutical Classes |