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Epirubicin Hydrochloride
Epirubicin Hydrochloride - 61703-347-35 - (EPIRUBICIN HYDROCHLORIDE)
Drug Information of Epirubicin Hydrochloride
| Product NDC: | 61703-347 |
| Proprietary Name: | Epirubicin Hydrochloride |
| Non Proprietary Name: | EPIRUBICIN HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/25mL & nbsp; EPIRUBICIN HYDROCHLORIDE |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Epirubicin Hydrochloride
| Product NDC: | 61703-347 |
| Labeler Name: | Hospira Worldwide, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050807 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060915 |
Package Information of Epirubicin Hydrochloride
| Package NDC: | 61703-347-35 |
| Package Description: | 25 mL in 1 VIAL, SINGLE-USE (61703-347-35) |
NDC Information of Epirubicin Hydrochloride
| NDC Code | 61703-347-35 |
| Proprietary Name | Epirubicin Hydrochloride |
| Package Description | 25 mL in 1 VIAL, SINGLE-USE (61703-347-35) |
| Product NDC | 61703-347 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | EPIRUBICIN HYDROCHLORIDE |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20060915 |
| Marketing Category Name | NDA |
| Labeler Name | Hospira Worldwide, Inc. |
| Substance Name | EPIRUBICIN HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/25mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
