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Epirubicin Hydrochloride
Epirubicin Hydrochloride - 25021-203-25 - (epirubicin hydrochloride)
Drug Information of Epirubicin Hydrochloride
| Product NDC: | 25021-203 |
| Proprietary Name: | Epirubicin Hydrochloride |
| Non Proprietary Name: | epirubicin hydrochloride |
| Active Ingredient(s): | 2 mg/mL & nbsp; epirubicin hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Epirubicin Hydrochloride
| Product NDC: | 25021-203 |
| Labeler Name: | Sagent Pharmaceutical |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065445 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20090908 |
Package Information of Epirubicin Hydrochloride
| Package NDC: | 25021-203-25 |
| Package Description: | 1 VIAL in 1 CARTON (25021-203-25) > 25 mL in 1 VIAL |
NDC Information of Epirubicin Hydrochloride
| NDC Code | 25021-203-25 |
| Proprietary Name | Epirubicin Hydrochloride |
| Package Description | 1 VIAL in 1 CARTON (25021-203-25) > 25 mL in 1 VIAL |
| Product NDC | 25021-203 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | epirubicin hydrochloride |
| Dosage Form Name | INJECTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20090908 |
| Marketing Category Name | ANDA |
| Labeler Name | Sagent Pharmaceutical |
| Substance Name | EPIRUBICIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
