FDA
Sodium Nitroprusside
The FDA lists this product in 25 strengths and forms.
Composition
- Active ingredients
- SODIUM NITROPRUSSIDE 25MG/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA210114-001 · Prescription
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA211934-001 · Discontinued
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA207426-001 · Prescription
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA209832-001 · Discontinued
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA210855-001 · Discontinued
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA208635-001 · Discontinued
- SODIUM NITROPRUSSIDE 50MG/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons** · InjectableNDA018581-001 · Discontinued
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA210763-001 · Prescription
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA214971-001 · Prescription
- SODIUM NITROPRUSSIDE 25MG/ML · InjectableANDA209493-001 · Prescription
- SODIUM NITROPRUSSIDE 25MG/ML · Injectable
At a glance
- Brand name
- Sodium Nitroprusside
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Sun Pharm
- Status
- Discontinued
- FDA approval
- 26 Nov 2018
- Application
- ANDA210467-001