FDA NDC Directory · JSON-LD · Markdown

Mannitol

NDC 84549-024 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameMANNITOL
Labeler / ManufacturerProPharma Distribution
Marketing categoryAbbreviated NDA (generic) · App ANDA080677
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMANNITOL (250 mg/mL)
Marketing started20000319
Package count1

External sources

Source: openFDA. Public-domain (CC0).