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Feraheme
Feraheme - 59338-775-01 - (ferumoxytol)
Drug Information of Feraheme
| Product NDC: | 59338-775 |
| Proprietary Name: | Feraheme |
| Non Proprietary Name: | ferumoxytol |
| Active Ingredient(s): | 510 mg/17mL & nbsp; ferumoxytol |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Feraheme
| Product NDC: | 59338-775 |
| Labeler Name: | AMAG Pharmaceuticals, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA022180 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20090713 |
Package Information of Feraheme
| Package NDC: | 59338-775-01 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (59338-775-01) > 17 mL in 1 VIAL, SINGLE-USE |
NDC Information of Feraheme
| NDC Code | 59338-775-01 |
| Proprietary Name | Feraheme |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (59338-775-01) > 17 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 59338-775 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ferumoxytol |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090713 |
| Marketing Category Name | NDA |
| Labeler Name | AMAG Pharmaceuticals, Inc. |
| Substance Name | FERUMOXYTOL NON-STOICHIOMETRIC MAGNETITE |
| Strength Number | 510 |
| Strength Unit | mg/17mL |
| Pharmaceutical Classes | Parental Iron Replacement [EPC] |
