# MAGNESIUM SULFATE

NDC: 47335-992
Generic name: magnesium sulfate heptahydrate
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20210801

FDA application: ANDA213917

## Active ingredients

- MAGNESIUM SULFATE HEPTAHYDRATE: 40 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"47335-992"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=47335-992
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=efadcb55-f935-4c60-b2e2-0a76b9194b50