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Epirubicin Hydrochloride
Epirubicin Hydrochloride - 0703-3069-11 - (Epirubicin Hydrochloride)
Drug Information of Epirubicin Hydrochloride
| Product NDC: | 0703-3069 |
| Proprietary Name: | Epirubicin Hydrochloride |
| Non Proprietary Name: | Epirubicin Hydrochloride |
| Active Ingredient(s): | 200 mg/100mL & 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: | 0703-3069 |
| Labeler Name: | Teva Parenteral Medicines, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA065331 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070809 |
Package Information of Epirubicin Hydrochloride
| Package NDC: | 0703-3069-11 |
| Package Description: | 1 VIAL, SINGLE-USE in 1 CARTON (0703-3069-11) > 100 mL in 1 VIAL, SINGLE-USE |
NDC Information of Epirubicin Hydrochloride
| NDC Code | 0703-3069-11 |
| Proprietary Name | Epirubicin Hydrochloride |
| Package Description | 1 VIAL, SINGLE-USE in 1 CARTON (0703-3069-11) > 100 mL in 1 VIAL, SINGLE-USE |
| Product NDC | 0703-3069 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Epirubicin Hydrochloride |
| Dosage Form Name | INJECTION, SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 20070809 |
| Marketing Category Name | ANDA |
| Labeler Name | Teva Parenteral Medicines, Inc. |
| Substance Name | EPIRUBICIN HYDROCHLORIDE |
| Strength Number | 200 |
| Strength Unit | mg/100mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
