FDA
Ondansetron Hydrochloride
The FDA lists this product in 60 strengths and forms.
Composition
- Active ingredients
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA076781-001 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA077368-001 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 8MG BASE · TabletANDA077517-002 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 24MG BASE · TabletANDA077517-003 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 4MG BASE · TabletANDA077517-001 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA077172-001 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA077473-001 · Prescription
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableThis page
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA090883-001 · Discontinued
- ONDANSETRON HYDROCHLORIDE EQ 2MG BASE/ML · InjectableANDA204906-001 · Discontinued
At a glance
- Brand name
- Ondansetron Hydrochloride
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Onesource Specialty
- Status
- Discontinued
- FDA approval
- 23 Apr 2008
- Application
- ANDA078257-001