FDA NDC Directory · JSON-LD · Markdown

MAGNESIUM SULFATE

NDC 51662-1352 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co LLC, DBA HealthFirst
Marketing categoryNew Drug Application (innovator) · App NDA020309
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsMAGNESIUM SULFATE HEPTAHYDRATE (40 mg/mL)
Marketing started20181221
Package count2

External sources

Source: openFDA. Public-domain (CC0).