# Zinc sulfate

NDC: 70069-692
Generic name: Zinc sulfate
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20240718

FDA application: ANDA216135

## Active ingredients

- ZINC SULFATE: 3 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-692"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-692
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c9d45d0e-a165-4112-81f9-c0e455572ecf