FDA
Mannitol 25%
The FDA lists this product in 10 strengths and forms.
Composition
- Active ingredients
- MANNITOL 12.5GM/50ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- MANNITOL 12.5GM/50ML · InjectableANDA087409-001 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableNDA005620-001 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableANDA080677-001 · Prescription
- MANNITOL 12.5GM/50ML · InjectableANDA087460-001 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableANDA089239-001 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableANDA089240-001 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableNDA016269-005 · Discontinued
- MANNITOL 12.5GM/50ML · InjectableNDA016269-006 · Prescription
- MANNITOL 12.5GM/50ML · InjectableThis page
- MANNITOL 12.5GM/50ML · InjectableANDA083051-001 · Discontinued
Official product information
Drugs@FDA lists the approved labels, letters and reviews for application ANDA086754.
At a glance
- Brand name
- Mannitol 25%
- Active substance
- mannitol
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Abraxis Pharm
- Status
- Discontinued
- FDA approval
- 10 Jun 1980
- Application
- ANDA086754-001