FDA NDC Directory · JSON-LD · Markdown

Selenious Acid

NDC 68083-660 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGland Pharma Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA219629
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSELENIUM (60 ug/mL)
Marketing started20250708
Package count1

External sources

Source: openFDA. Public-domain (CC0).