Selenium
- Product NDC
- 0517-6510
- 11-digit product format
- 005176510
- Labeler code
- 0517
- Product ID
- 0517-6510_08d7aacf-6d5c-4873-87bc-25725c9ec7b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Selenium
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- American Regent, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-30
- Marketing end
- 2021-03-31
- Substance
- SELENIOUS ACID
- Active strength
- 65 ug/mL
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0517-6510-25 | 00517651025 | 25 VIAL, SINGLE-DOSE in 1 TRAY (0517-6510-25) > 10 mL in 1 VIAL, SINGLE-DOSE | 1990-09-30 | 2021-03-31 | No | No | Current |