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Mannitol

NDC 0409-4031 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMANNITOL
Labeler / ManufacturerHospira, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA016269
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMANNITOL (12.5 g/50mL)
Marketing started20041130
Package count1

External sources

Source: openFDA. Public-domain (CC0).