FDA NDC Directory · JSON-LD · Markdown

50% MAGNESIUM SULFATE

NDC 51662-1235 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerHF Acquisition Co. LLC, DBA Health First
Marketing categoryAbbreviated NDA (generic) · App ANDA075151
Dosage form / routeINJECTION, SOLUTION · INTRAMUSCULAR INTRAVENOUS
Active ingredientsMAGNESIUM SULFATE HEPTAHYDRATE (500 mg/mL)
Marketing started20180825
Package count2

External sources

Source: openFDA. Public-domain (CC0).