# Selenious Acid

NDC: 68083-660
Generic name: Selenious Acid
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20250708

FDA application: ANDA219629

## Active ingredients

- SELENIUM: 60 ug/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68083-660"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-660
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1be55144-afc8-45ff-82a9-162a6279d2a8