FDA
Daunorubicin Hydrochloride
The FDA lists this product in 8 strengths and forms.
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 · InjectableANDA064212-001 · Discontinued
- DAUNORUBICIN HYDROCHLORIDE EQ 50MG BASE/VIAL · InjectableANDA064212-002 · Discontinued
- DAUNORUBICIN HYDROCHLORIDE EQ 5MG BASE/ML · InjectableNDA050731-001 · Prescription
- DAUNORUBICIN HYDROCHLORIDE EQ 5MG BASE/ML · InjectableANDA208759-001 · Prescription
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL · InjectableANDA065000-001 · Prescription
- DAUNORUBICIN HYDROCHLORIDE EQ 20MG BASE/VIAL · InjectableThis page
- DAUNORUBICIN HYDROCHLORIDE EQ 5MG BASE/VIAL · InjectableANDA065034-001 · Discontinued
- DAUNORUBICIN HYDROCHLORIDE EQ 5MG BASE/ML · InjectableANDA065035-001 · Prescription
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA206195.
At a glance
- Brand name
- Daunorubicin Hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Hisun Pharm Hangzhou
- Status
- Discontinued
- FDA approval
- 25 Apr 2019
- Application
- ANDA206195-001