FDA NDC Directory · JSON-LD · Markdown

Selenious Acid

NDC 0517-6502 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerAmerican Regent, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA209379
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSELENIUM (6 ug/mL)
Marketing started20220328
Package count1

External sources

Source: openFDA. Public-domain (CC0).