NDC 73309-013 - 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
- 73309-013
- Package NDCs from labels
- 73309-013-01
- Manufacturer
- BLUEBAY SHANDONG CO.,LTD
- Effective date
- 2019-08-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prednisolone Sodium Phosphate - BLUEBAY SHANDONG CO.,LTD | BLUEBAY SHANDONG CO.,LTD | 2019-08-21 | BULK INGREDIENT |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 73309-013-01 | Prednisolone Sodium Phosphate | 5 kg in 1 CANISTER | POWDER | 5 | 1 |
DailyMed Dashboard NDC Coverage#
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.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Sulfacetamide Sodium and Prednisolone Sodium Phosphate | SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE | Bausch & Lomb Incoporated | 9ec403eb-b5df-4e41-9e17-9d9d8ecac3f3 | 2023-08-01 | Warnings, Adverse reactions | IV021NXA9J |
| PREDNISOLONE SODIUM PHOSPHATE | PREDNISOLONE SODIUM PHOSPHATE | Bausch & Lomb Incorporated | 8a7f0f2a-3a48-4488-89cd-3e91c3b1365f | 2023-04-17 | Warnings, Adverse reactions | IV021NXA9J |
| Prednisolone Sodium Phosphate | PREDNISOLONE SODIUM PHOSPHATE | Proficient Rx LP | 14b7f41b-4df1-42cb-bd1b-c74b28de2670 | 2021-01-01 | Warnings, Adverse reactions | IV021NXA9J |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.