United States · FDA National Drug Code directory
Selenious Acid
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 0517-6560_4f6657ea-8dfd-4a74-8a36-9855ca7fd34a
- Product NDC
- 0517-6560
- Form
- INJECTION, SOLUTION
- Composition / generic term
- Selenious Acid
- Labeler
- American Regent, Inc.
- Marketing category
- NDA
- Marketing start / end (source format)
- 20190701
- Source listing expiry
- 20261231
Source-listed ingredients
- SELENIUM — 60 ug/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 5 VIAL, PHARMACY BULK PACKAGE in 1 BOX (0517-6560-05) / 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (0517-6560-01) · 0517-6560-05
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →