FDA
Dobutamine Hydrochloride
The FDA lists this product in 12 strengths and forms.
Composition
- Active ingredients
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074086-001 · Prescription
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074206-001 · Discontinued
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074277-001 · Prescription
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074279-001 · Discontinued
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableThis page
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA216131-001 · Prescription
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074114-001 · Discontinued
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074381-001 · Discontinued
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074995-001 · Discontinued
- DOBUTAMINE HYDROCHLORIDE EQ 12.5MG BASE/ML · InjectableANDA074098-001 · Discontinued
At a glance
- Brand name
- Dobutamine Hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Luitpold
- Status
- Discontinued
- FDA approval
- 25 Jun 1998
- Application
- ANDA074545-001