Azathioprine
- Product NDC
- 68071-3772
- 11-digit product format
- 680713772
- Labeler code
- 68071
- Product ID
- 68071-3772_2b9f91b9-795a-65e7-e063-6294a90a3680
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azathioprine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA077621
- Marketing category
- ANDA
- Marketing start
- 2007-07-11
- Substance
- AZATHIOPRINE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Nucleic Acid Synthesis Inhibitors [MoA], Nucleosides [CS], Purine Antimetabolite [EPC], Purines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| MRK240IY2L | AZATHIOPRINE | 446-86-6 | AZATHIOPRINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68071-3772-6 | 68071377206 | 60 TABLET in 1 BOTTLE (68071-3772-6) | 60 tablet | 2025-01-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Azathioprine Tablets, USP | NuCare Pharmaceuticals, Inc. | 2025-01-13 | HUMAN PRESCRIPTION DRUG LABEL | 1 |