# 50% MAGNESIUM SULFATE

NDC: 51662-1235
Generic name: 50% MAGNESIUM SULFATE
Labeler / Manufacturer: HF Acquisition Co. LLC, DBA Health First
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20180825

FDA application: ANDA075151

## Active ingredients

- MAGNESIUM SULFATE HEPTAHYDRATE: 500 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1235"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1235
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7446d09b-10fe-7765-e053-2a91aa0a56a8