Azathioprine
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Azathioprine
- Generic name
- AZATHIOPRINE
- Manufacturer
- Zydus Lifesciences Limited
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d65bc662-2ae8-4ddb-acc8-f616e72e6140
- SPL ID
- b1337f9b-c728-4b49-b29a-4f593c100f9c
- Version
- 9
- Effective date
- 2024-11-25
- Source export date
- 2026-10-12
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 03:08:54
| Harmonized routes |
|---|
| ORAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application applno | ANDA | 077621 | derived:openfda.application_number |
| application number | ANDA077621 | openfda.application_number | |
| brand name | Azathioprine | openfda.brand_name | |
| generic name | AZATHIOPRINE | openfda.generic_name | |
| manufacturer name | Zydus Lifesciences Limited | openfda.manufacturer_name | |
| ndc | package | 65841-602-05 | openfda.package_ndc |
| ndc | package | 65841-602-01 | openfda.package_ndc |
| ndc | product | 65841-602 | openfda.product_ndc |
| ndc11 | package | 65841060205 | derived:openfda.package_ndc |
| ndc11 | package | 65841060201 | derived:openfda.package_ndc |
| rxcui | 197388 | openfda.rxcui | |
| spl id | b1337f9b-c728-4b49-b29a-4f593c100f9c | id | |
| spl set id | d65bc662-2ae8-4ddb-acc8-f616e72e6140 | set_id | |
| unii | MRK240IY2L | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.