Selenious Acid
- Product NDC
- 69784-840
- 11-digit product format
- 697840840
- Labeler code
- 69784
- Product ID
- 69784-840_0e72ffb7-8a0c-4a1e-96a8-dc9ee085f7d2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Selenious Acid
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Woodward Pharma Services LLC
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-03-15
- Marketing end
- 0000-00-00
- Substance
- SELENIUM
- Active strength
- 40 ug/mL
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69784-840 | SELENIOUS ACID INJECTION, SOLUTION [WOODWARD PHARMA SERVICES LLC] | 1 | Legacy NDC | 20220416_33e42ead-bbf7-4aa7-b6cb-c4b6b85a240e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69784-840-05 | 69784084005 | 5 VIAL, PHARMACY BULK PACKAGE in 1 BOX (69784-840-05) > 10 mL in 1 VIAL, PHARMACY BULK PACKAGE (69784-840-01) | 2022-03-15 | 0000-00-00 | No | No | Current |