NDC 70518-3263-2 - 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
- 70518-3263
- Requested NDC
- 70518-3263-2
- Package NDCs from labels
- 70518-3263-0, 70518-3263-2, 70518-3263-1, 70518-3263-3, 70518-3263-4
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2024-03-14
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Methotrexate - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-03-14 | 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 |
|---|---|---|---|---|---|---|
| 2357252a-b7fc-4192-e063-6394a90abe8e | 912e2a80-bb07-457f-8944-d9f672ef8081 | 2024-09-30 | Boxed warning, Warnings, Adverse reactions | 912e2a80-bb07-457f-8944-d9f672ef8081 | ||
| Methotrexate | METHOTREXATE | Proficient Rx LP | a76808f0-38a7-4b54-a4fb-3584f9058ae5 | 2024-08-01 | Boxed warning, Warnings, Adverse reactions | ANDA213343 105585 3IG1E710ZN |
| METHOTREXATE | METHOTREXATE | Alembic Pharmaceuticals Limited | ff55c573-dc84-4ff3-9d10-2b24c47dd679 | 2024-06-07 | Boxed warning, Warnings, Adverse reactions | 105585 3IG1E710ZN |
| 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 3IG1E710ZN |
| Methotrexate | METHOTREXATE SODIUM | Fresenius Kabi USA, LLC | b585f621-f6c9-4735-ab61-bd1b401f3df0 | 2021-03-24 | Boxed warning, Adverse reactions | 3IG1E710ZN |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.