Azathioprine
NDC 70771-1139, Azathioprine, tablet, from Zydus Lifesciences Limited.
- Product NDC
- 70771-1139
- 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/70771-1139 \ -H "Authorization: Bearer $HDEV_API_KEY"
Product
Active ingredients and packages
Active ingredients
- AZATHIOPRINE25 mg/1
Pharmacologic classes
Nucleic Acid Synthesis Inhibitors [MoA]; Nucleosides [CS]; Purine Antimetabolite [EPC]; Purines [CS]
| Package NDC | NDC-11 | Package |
|---|---|---|
| 70771-1139-1 | 70771113901 | 100 TABLET in 1 BOTTLE (70771-1139-1) |
| 70771-1139-5 | 70771113905 | 500 TABLET in 1 BOTTLE (70771-1139-5) |
Linked data
RxNorm, label and prices
RxNorm concepts
Related lookups
FDA label sections
GET /v1/drugs/labels/89b272f0-ef5c-49e4-820f-fcd7ea8ef066
Use it
Look up 70771-1139 from code or an agent
curl https://api.healthcare.dev/v1/drugs/ndc/70771-1139 \ -H "Authorization: Bearer $HDEV_API_KEY"
Using the healthcare.dev MCP server, look up NDC 70771-1139. 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.