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NDC 65649-0231-41 Azasan 75 mg/1 Details
Azasan 75 mg/1
Azasan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Salix Pharmaceuticals. The primary component is AZATHIOPRINE.
MedlinePlus Drug Summary
Azathioprine is used with other medications to prevent transplant rejection (attack of the transplanted organ by the immune system) in people who received kidney transplants. It is also used to treat severe rheumatoid arthritis (a condition in which the body attacks its own joints, causing pain, swelling, and loss of function) when other medications and treatments have not helped. Azathioprine is in a class of medications called immunosuppressants. It works by decreasing the activity of the body's immune system so it will not attack the transplanted organ or the joints.
Related Packages: 65649-0231-41Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Azathioprine
Product Information
| NDC | 65649-0231 |
|---|---|
| Product ID | 65649-231_0cceeb5c-3f54-cca0-e063-6394a90a3b95 |
| Associated GPIs | 99406010000315 |
| GCN Sequence Number | 051793 |
| GCN Sequence Number Description | azathioprine TABLET 75 MG ORAL |
| HIC3 | Z2E |
| HIC3 Description | IMMUNOSUPPRESSIVES |
| GCN | 19170 |
| HICL Sequence Number | 004523 |
| HICL Sequence Number Description | AZATHIOPRINE |
| Brand/Generic | Brand |
| Proprietary Name | Azasan |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Azathioprine |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 75 |
| Active Ingredient Units | mg/1 |
| Substance Name | AZATHIOPRINE |
| Labeler Name | Salix Pharmaceuticals |
| Pharmaceutical Class | Nucleic Acid Synthesis Inhibitors [MoA], Nucleosides [CS], Purine Antimetabolite [EPC], Purines [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA075252 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 65649-0231-41 (65649023141)
| NDC Package Code | 65649-231-41 |
|---|---|
| Billing NDC | 65649023141 |
| Package | 100 TABLET in 1 BOTTLE (65649-231-41) |
| Marketing Start Date | 2003-04-01 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |