NDC 0951-5442-05 - Prednisone
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
- 0951-5442
- Requested NDC
- 0951-5442-05
- Package NDCs from labels
- 0951-5442-01, 0951-5442-05, 0951-5442-10
- Manufacturer
- Watson Pharma, Inc.
- Effective date
- 2009-01-12
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Prednisone Tablets USP Revised: April 2008 Rx only 2000260-01 | Watson Pharma, Inc. | 2009-01-12 | HUMAN PRESCRIPTION DRUG LABELING |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| Prednisone | ACTIVE INGREDIENT | VB0R961HZT | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| Prednisone | ACTIVE MOIETY | VB0R961HZT | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| anhydrous lactose | INACTIVE INGREDIENT | 3SY5LH9PMK | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| colloidiol silicon dioxide | INACTIVE INGREDIENT | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | ||
| crospovidone | INACTIVE INGREDIENT | 68401960MK | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| docusate sodium | INACTIVE INGREDIENT | F05Q2T2JA0 | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| FD & C Yellow #6 | INACTIVE INGREDIENT | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | ||
| magnesium stearate | INACTIVE INGREDIENT | 70097M6I30 | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 | |
| sodium benzoate | INACTIVE INGREDIENT | OJ245FE5EU | PREDNISONE TABLET [WATSON PHARMA, INC.] | 4 |
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 |
|---|---|---|---|---|---|---|
| 37CA5A19-DF10-3C3D-985D-75A27C82B2F7 | A784F545-F209-46D4-9350-AE64FAD9E07C | 2009-01-12 | Warnings, Adverse reactions | 37CA5A19-DF10-3C3D-985D-75A27C82B2F7 A784F545-F209-46D4-9350-AE64FAD9E07C |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.