Composition
- Active ingredients
- ONDANSETRON 8MG
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA077717-002 · Discontinued
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA077717-001 · Discontinued
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA209389-002 · Prescription
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA209389-001 · Prescription
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA090469-001 · Prescription
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA090469-002 · Prescription
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA078139-002 · Discontinued
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA078139-001 · Discontinued
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA078152-001 · Prescription
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA078152-002 · Prescription
- ONDANSETRON 8MG · Tablet, orally disintegratingANDA076810-002 · Discontinued
- ONDANSETRON 4MG · Tablet, orally disintegratingANDA076810-001 · Discontinued
At a glance
- Brand name
- Ondansetron
- Route
- Oral
- Dosage form
- Tablet, orally disintegrating
- Applicant
- Barr
- Status
- Discontinued
- FDA approval
- 25 Jun 2007
- Application
- ANDA076693-002