FDA
Epirubicin Hydrochloride
The FDA lists this product in 32 strengths and forms.
Composition
- Active ingredients
- EPIRUBICIN HYDROCHLORIDE 50MG/VIAL
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- EPIRUBICIN HYDROCHLORIDE 200MG/100ML (2MG/ML) · InjectableANDA090075-002 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 50MG/25ML (2MG/ML) · InjectableANDA090075-001 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 50MG/25ML (2MG/ML) · InjectableANDA065331-001 · Prescription
- EPIRUBICIN HYDROCHLORIDE 200MG/100ML (2MG/ML) · InjectableANDA065331-002 · Prescription
- EPIRUBICIN HYDROCHLORIDE 150MG/75ML (2MG/ML) · InjectableANDA065343-003 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 10MG/5ML (2MG/ML) · InjectableANDA065343-001 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 200MG/100ML (2MG/ML) · InjectableANDA065343-004 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 50MG/25ML (2MG/ML) · InjectableANDA065343-002 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 50MG/25ML (2MG/ML) · InjectableANDA065411-002 · Discontinued
- EPIRUBICIN HYDROCHLORIDE 200MG/100ML (2MG/ML) · Injectable
At a glance
- Brand name
- Epirubicin Hydrochloride
- Route
- Intravenous
- Dosage form
- Powder
- Applicant
- Hospira
- Status
- Discontinued
- FDA approval
- 15 Sept 2006
- Application
- NDA050807-001