NDC 79481-0149-01 - meijer EXTRA STRENGTH Pain Relief PM Caplet
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
- 79481-0149
- Requested NDC
- 79481-0149-01
- Package NDCs from labels
- 79481-0149-5, 79481-0149-1, 79481-0149-2, 79481-0149-3, 79481-0149-01
- Manufacturer
- Meijer, Inc.
- Effective date
- 2025-02-17
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| meijer EXTRA STRENGTH Pain Relief PM Caplet | Meijer, Inc. | 2025-02-17 | HUMAN OTC DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 79481-0149-1 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 79481-0149-1 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-2 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 2 in 1 CARTON | TABLET | 2 | 3 | |
| 79481-0149-2 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 100 in 1 BOTTLE | TABLET | 100 | 3 | |
| 79481-0149-3 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-3 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 24 in 1 BOTTLE | TABLET | 24 | 3 | |
| 79481-0149-5 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 1 in 1 CARTON | TABLET | 1 | 3 | |
| 79481-0149-5 | meijer EXTRA STRENGTH Pain Relief PM Caplet | 50 in 1 BOTTLE | TABLET | 50 | 3 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 79481-0149 | MEIJER EXTRA STRENGTH PAIN RELIEF PM CAPLET (ACETAMINOPHEN, DIPHENHYDRAMINE HYDROCHLORIDE) TABLET [MEIJER, INC.] | 3 | Current NDC, 8 package rows | 20250313_1bee7e4f-1813-1bdf-e063-6294a90a6a32.zip |
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.