Azathioprine
NDC 65841-602, Azathioprine, tablet, from Zydus Lifesciences Limited.
- Product NDC
- 65841-602
- Status
- Listed
- Labeler
- Zydus Lifesciences Limited
- Dosage form
- TABLET
- Route
- ORAL
- Product type
- HUMAN PRESCRIPTION DRUG
- Marketing category
- ANDA
- Application
- ANDA077621
- DEA schedule
- None
curl https://api.healthcare.dev/v1/drugs/ndc/65841-602 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AZATHIOPRINE50 mg/1
Pharmacologic classes
Nucleic Acid Synthesis Inhibitors [MoA]; Nucleosides [CS]; Purine Antimetabolite [EPC]; Purines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 65841-602-01 | 65841060201 | 100 TABLET in 1 BOTTLE (65841-602-01) |
| 65841-602-05 | 65841060205 | 500 TABLET in 1 BOTTLE (65841-602-05) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/d65bc662-2ae8-4ddb-acc8-f616e72e6140
Use it
Look up 65841-602 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/65841-602 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 65841-602. Tell me the product, its labeler, dosage form and route, its packages, and the RxNorm concepts it maps to.
Source: FDA, release 2026-10-23. Public domain. Reference data, not medical advice.