NDC 58177-912 - Prednisolone
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
- 58177-912
- Package NDCs from labels
- 58177-912-03
- Manufacturer
- Physicians Total Care, Inc.
- Effective date
- 2010-01-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prednisolone - Physicians Total Care, Inc. | Physicians Total Care, Inc. | 2010-01-05 | HUMAN PRESCRIPTION DRUG LABEL |
| Prednisolone - KV Pharmaceuticals | KV Pharmaceuticals | 2006-12-26 | Human Prescription Drug Label |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 58177-912-03 | Prednisolone | 120 mL in 1 BOTTLE | SYRUP | 120 | 1 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58177-912-03 | ML - Milliliter | 58177-912 | ebf3fac1-7860-4a8f-9c2d-1744fcc70a94 | 1 | 2013-02-13 |
DailyMed Socrata Ingredients#
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.