NDC 51672-4258-01 - Acetaminophen 250 mg and Ibuprofen 125 mg
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
- 51672-4258
- Requested NDC
- 51672-4258-01
- Package NDCs from labels
- 51672-4258-4, 51672-4258-1, 51672-4258-01
- Manufacturer
- Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd.
- Effective date
- 2026-03-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Acetaminophen and Ibuprofen (NSAID) Tablets 250mg/125mg | Sun Pharmaceutical Industries, Inc. | Taro Pharmaceutical Industries Ltd. | 2026-03-10 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 51672-4258-1 | Acetaminophen 250 mg and Ibuprofen 125 mg | 1 in 1 CARTON | TABLET | 1 | 4 | |
| 51672-4258-1 | Acetaminophen 250 mg and Ibuprofen 125 mg | 216 in 1 BOTTLE | TABLET | 216 | 4 | |
| 51672-4258-4 | Acetaminophen 250 mg and Ibuprofen 125 mg | 1 in 1 CARTON | TABLET | 1 | 4 | |
| 51672-4258-4 | Acetaminophen 250 mg and Ibuprofen 125 mg | 72 in 1 BOTTLE | TABLET | 72 | 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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.