NDC 51660-420 - Ibuprofen
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
- 51660-420
- Manufacturer
- McKesson Packaging Services Business Unit of McKesson Corporation
- Effective date
- 2009-12-03
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Ibuprofen - McKesson Packaging Services Business Unit of McKesson Corporation | McKesson Packaging Services Business Unit of McKesson Corporation | 2009-12-03 | HUMAN OTC DRUG LABEL |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| IBUPROFEN | ACTIVE INGREDIENT | WK2XYI10QM | IBUPROFEN TABLET, SUGAR COATED [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 | |
| IBUPROFEN | ACTIVE MOIETY | WK2XYI10QM | IBUPROFEN TABLET, SUGAR COATED [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | IBUPROFEN TABLET, SUGAR COATED [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 | |
| PROPYLENE GLYCOL | INACTIVE INGREDIENT | 6DC9Q167V3 | IBUPROFEN TABLET, SUGAR COATED [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 | |
| STARCH, CORN | INACTIVE INGREDIENT | O8232NY3SJ | IBUPROFEN TABLET, SUGAR COATED [MCKESSON PACKAGING SERVICES BUSINESS UNIT OF MCKESSON CORPORATION] | 1 |
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.