NDC 81033-021-05 - prednisoLONE sodium phosphate
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
- 81033-021
- Requested NDC
- 81033-021-05
- Package NDCs from labels
- 81033-021-05, 81033-021-54
- Manufacturer
- Kesin Pharma
- Effective date
- 2026-03-27
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| prednisoLONE sodium phosphate - Kesin Pharma | Kesin Pharma | 2026-03-27 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 81033-021-05 | prednisoLONE sodium phosphate | 5 mL in 1 CUP, UNIT-DOSE | SOLUTION | 5 | 1 | |
| 81033-021-54 | prednisoLONE sodium phosphate | 50 in 1 CARTON | SOLUTION | 50 | 1 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 81033-021-05 | ML - Milliliter | 81033-021 | 7dd889e7-cca9-4036-9034-7aa49a2f91c0 | 1 | 2026-04-20 |
| 81033-021-54 | ML - Milliliter | 81033-021 | e0414667-e663-4472-90cf-995197a97722 | 1 | 2026-04-20 |
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.
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.