# zinc sulfate

NDC: 70710-1876
Generic name: zinc sulfate injection,
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20231207

FDA application: ANDA217074

## Active ingredients

- ZINC SULFATE: 1 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70710-1876"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1876
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=95aa8437-10bc-4205-939f-d21d8fa52a00