FDA NDC Directory · JSON-LD · Markdown

MANNITOL

NDC 51662-1468 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA016269
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMANNITOL (12.5 g/50mL)
Marketing started20191213
Package count2

External sources

Source: openFDA. Public-domain (CC0).