Composition
- Active ingredients
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA050484-001 · Discontinued
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL · InjectableThis page
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL · InjectableANDA064103-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA061876.
Prognia shows this product information for reference and learning. It is not treatment advice and can lag behind the official text. Always check the current product information and local protocols before prescribing.
At a glance
- Brand name
- Cerubidine
- Active substance
- daunorubicin hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Sanofi Aventis US
- Status
- Discontinued
- FDA approval
- 5 Feb 1980
- Application
- ANDA061876-001