FDA
Doxorubicin Hydrochloride
The FDA lists this product in 35 strengths and forms.
Composition
- Active ingredients
- DOXORUBICIN HYDROCHLORIDE 20MG/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DOXORUBICIN HYDROCHLORIDE 2MG/ML · InjectableANDA091495-001 · Prescription
- DOXORUBICIN HYDROCHLORIDE 10MG/VIAL · InjectableANDA200170-001 · Discontinued
- DOXORUBICIN HYDROCHLORIDE 50MG/VIAL · InjectableANDA200170-002 · Prescription
- DOXORUBICIN HYDROCHLORIDE 2MG/ML · InjectableANDA209825-001 · Prescription
- DOXORUBICIN HYDROCHLORIDE 200MG/100ML · InjectableNDA050629-002 · Prescription
- DOXORUBICIN HYDROCHLORIDE 150MG/75ML · InjectableNDA050629-003 · Discontinued
- DOXORUBICIN HYDROCHLORIDE 2MG/ML · InjectableNDA050629-001 · Prescription
- DOXORUBICIN HYDROCHLORIDE 50MG/VIAL · InjectableANDA062921-003 · Prescription
- DOXORUBICIN HYDROCHLORIDE 10MG/VIAL · InjectableANDA062921-001 · Prescription
- DOXORUBICIN HYDROCHLORIDE 20MG/VIAL · InjectableANDA062921-002 · Prescription
At a glance
- Brand name
- Doxorubicin Hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Hisun Pharm Hangzhou
- Status
- Discontinued
- FDA approval
- 13 May 2019
- Application
- ANDA206062-001