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epirubicin hydrochloride
epirubicin hydrochloride - 59762-5091-1 - (epirubicin hydrochloride)
Drug Information of epirubicin hydrochloride
| Product NDC: | 59762-5091 |
| 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, SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of epirubicin hydrochloride
| Product NDC: | 59762-5091 |
| Labeler Name: | Greenstone, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050778 |
| Marketing Category: | NDA AUTHORIZED GENERIC |
| Start Marketing Date: | 19990915 |
Package Information of epirubicin hydrochloride
| Package NDC: | 59762-5091-1 |
| Package Description: | 25 mL in 1 VIAL, SINGLE-USE (59762-5091-1) |
NDC Information of epirubicin hydrochloride
| NDC Code | 59762-5091-1 |
| Proprietary Name | epirubicin hydrochloride |
| Package Description | 25 mL in 1 VIAL, SINGLE-USE (59762-5091-1) |
| Product NDC | 59762-5091 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | epirubicin hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19990915 |
| Marketing Category Name | NDA AUTHORIZED GENERIC |
| Labeler Name | Greenstone, LLC |
| Substance Name | EPIRUBICIN HYDROCHLORIDE |
| Strength Number | 2 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
