NDC 17478-988-02 - Doxercalciferol
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 17478-988
- Requested NDC
- 17478-988-02
- Package NDCs from labels
- 17478-988-02, 17478-988-12, 17478-988-22
- Manufacturer
- Akorn | Akorn Operating Company LLC
- Effective date
- 2022-01-26
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Doxercalciferol - Akorn | Akorn Operating Company LLC | Akorn | Akorn Operating Company LLC | 2022-01-26 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Doxercalciferol | ACTIVE INGREDIENT | 3DIZ9LF5Y9 | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Doxercalciferol | ACTIVE MOIETY | 3DIZ9LF5Y9 | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Alcohol | INACTIVE INGREDIENT | 3K9958V90M | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Butylated Hydroxytoluene | INACTIVE INGREDIENT | 1P9D0Z171K | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Edetate Disodium | INACTIVE INGREDIENT | 7FLD91C86K | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Polysorbate 20 | INACTIVE INGREDIENT | 7T1F30V5YH | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Sodium Chloride | INACTIVE INGREDIENT | 451W47IQ8X | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Sodium Phosphate, Dibasic, Heptahydrate | INACTIVE INGREDIENT | 70WT22SF4B | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 | |
| Sodium Phosphate, Monobasic, Monohydrate | INACTIVE INGREDIENT | 593YOG76RN | DOXERCALCIFEROL INJECTION, SOLUTION [AKORN, INC.] | 3 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.