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Daunorubicin Hydrochloride
Daunorubicin Hydrochloride - 55390-805-10 - (Daunorubicin Hydrochloride)
Drug Information of Daunorubicin Hydrochloride
| Product NDC: | 55390-805 |
| Proprietary Name: | Daunorubicin Hydrochloride |
| Non Proprietary Name: | Daunorubicin Hydrochloride |
| Active Ingredient(s): | 5 mg/mL & nbsp; Daunorubicin Hydrochloride |
| Administration Route(s): | INTRAVENOUS |
| Dosage Form(s): | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Daunorubicin Hydrochloride
| Product NDC: | 55390-805 |
| Labeler Name: | Bedford Laboratories |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA064103 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 19960628 |
Package Information of Daunorubicin Hydrochloride
| Package NDC: | 55390-805-10 |
| Package Description: | 10 VIAL in 1 BOX (55390-805-10) > 4 mL in 1 VIAL |
NDC Information of Daunorubicin Hydrochloride
| NDC Code | 55390-805-10 |
| Proprietary Name | Daunorubicin Hydrochloride |
| Package Description | 10 VIAL in 1 BOX (55390-805-10) > 4 mL in 1 VIAL |
| Product NDC | 55390-805 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Daunorubicin Hydrochloride |
| Dosage Form Name | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
| Route Name | INTRAVENOUS |
| Start Marketing Date | 19960628 |
| Marketing Category Name | ANDA |
| Labeler Name | Bedford Laboratories |
| Substance Name | DAUNORUBICIN |
| Strength Number | 5 |
| Strength Unit | mg/mL |
| Pharmaceutical Classes | Anthracycline Topoisomerase Inhibitor [EPC],Anthracyclines [Chemical/Ingredient],Topoisomerase Inhibitors [MoA] |
