Selenious acid
- Product NDC
- 87944-001
- 11-digit product format
- 879440001
- Labeler code
- 87944
- Product ID
- 87944-001_5a55c7ab-4db1-340c-e063-6394a90a3b31
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- selenious acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Resor Labs
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-10-01
- Substance
- SELENIOUS ACID
- Active strength
- 40 ug/mL
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Selenious acid
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| SELENIOUS ACID | 40 ug/mL |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 87944-001-01 | 87944000101 | 20 mL in 1 VIAL (87944-001-01) | 20 ml | 2026-10-01 | No | No | Current |