AZATHIOPRINE
- Product NDC
- 60219-1076
- 11-digit product format
- 602191076
- Labeler code
- 60219
- Product ID
- 60219-1076_7b890b18-936a-43f1-9980-e94a417762f6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Azathioprine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Amneal Pharmaceuticals NY LLC
- Application
- ANDA074069
- Marketing category
- ANDA
- Marketing start
- 2015-02-02
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- AZATHIOPRINE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AZATHIOPRINE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MRK240IY2L |
| Rxcui | 197388, 359228, 359229 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 60219-1076-1 | AZATHIOPRINE | 100 in 1 BOTTLE | TABLET | 100 | | 16 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60219-1076 | AZATHIOPRINE TABLET [AMNEAL PHARMACEUTICALS NY LLC] | 15 | Current NDC, Legacy NDC, 1 package rows | 20240910_59f3219f-898f-4d05-a430-c2b3f5255af1.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60219-1076-1 | 60219107601 | 100 TABLET in 1 BOTTLE (60219-1076-1) | 100 tablet | 2015-02-02 | 0000-00-00 | No | No | Current |