| Product NDC: | 0517-0234 |
| 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: | 0517-0234 |
| Labeler Name: | American Regent, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA040024 |
| Marketing Category: | NDA |
| Start Marketing Date: | 19960301 |
| Package NDC: | 0517-0234-10 |
| Package Description: | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-0234-10) > 2 mL in 1 VIAL, SINGLE-DOSE |
| NDC Code | 0517-0234-10 |
| Proprietary Name | Dexferrum |
| Package Description | 10 VIAL, SINGLE-DOSE in 1 BOX (0517-0234-10) > 2 mL in 1 VIAL, SINGLE-DOSE |
| Product NDC | 0517-0234 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | iron dextran |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19960301 |
| Marketing Category Name | NDA |
| Labeler Name | American Regent, Inc. |
| Substance Name | IRON DEXTRAN |
| Strength Number | 50 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes |