NDC 70518-3544-01 - Azathioprine
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
- 70518-3544
- Requested NDC
- 70518-3544-01
- Package NDCs from labels
- 70518-3544-1, 70518-3544-0, 70518-3544-01
- Manufacturer
- REMEDYREPACK INC.
- Effective date
- 2026-04-13
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Azathioprine Tablets, USP Scored Tablets PRODUCT INFORMATION Rx only | REMEDYREPACK INC. | 2026-04-13 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 70518-3544-0 | Azathioprine | 100 in 1 BOX | TABLET | 100 | 4 | |
| 70518-3544-1 | Azathioprine | 1 in 1 POUCH | TABLET | 1 | 4 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 70518-3544 | AZATHIOPRINE TABLET [REMEDYREPACK INC.] | 2 | Current NDC, Legacy NDC, 2 package rows | 20240116_f251f372-c881-483e-8035-c6a8a6bfb4e8.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.
| 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 |
| AZATHIOPRINE | AZATHIOPRINE | Amneal Pharmaceuticals NY LLC | c49b7cc5-0eed-43b7-b7ad-cbb1b6f0cd2c | 2021-02-02 | Boxed warning, Warnings, Adverse reactions | 197388 MRK240IY2L |
| AZATHIOPRINE | AZATHIOPRINE | Aphena Pharma Solutions - Tennessee, LLC | 2f994aed-f8e7-4967-a167-b22b783b4192 | 2018-09-05 | Boxed warning, Warnings, Adverse reactions | 197388 MRK240IY2L |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.