# Selenious Acid

NDC: 0517-6502
Generic name: Selenious Acid
Labeler / Manufacturer: American Regent, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220328

FDA application: NDA209379

## Active ingredients

- SELENIUM: 6 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0517-6502"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0517-6502
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=49324999-50e3-43ed-a8dd-156d6dbedd9f