NDC 70518-1398-5 - Methotrexate
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
- 70518-1398
- Requested NDC
- 70518-1398-5
- Package NDCs from labels
- 70518-1398-0, 70518-1398-1, 70518-1398-2, 70518-1398-3, 70518-1398-5, 70518-1398-4
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2024-07-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Methotrexate - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-07-15 | HUMAN PRESCRIPTION DRUG LABEL |
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 |
|---|---|---|---|---|---|---|
| Pure Cornstarch Baby | CORN STARCH | Walgreen Company | d0e9bd13-b568-4f7e-b036-8d23e71ad8bf | 2024-03-25 | Warnings | O8232NY3SJ |
| Methotrexate | METHOTREXATE SODIUM | Bryant Ranch Prepack | c7592288-ac24-46c6-8cec-9abe23d7e81e | 2023-12-07 | Boxed warning, Warnings, Adverse reactions | 105585 |
| Methotrexate | METHOTREXATE | Hikma Pharmaceuticals USA Inc. | 3989d30d-56e5-4e8d-9379-c30fecc894f2 | 2023-04-17 | Boxed warning, Warnings, Adverse reactions | YL5FZ2Y5U1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.