NDC 71610-306 Azathioprine
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 71610 - Aphena Pharma Solutions - Tennessee, Llc
- 71610-306 - Azathioprine
Product Characteristics
Product Packages
NDC Code 71610-306-60
Package Description: 90 TABLET in 1 BOTTLE
Product Details
What is NDC 71610-306?
What are the uses for Azathioprine?
Which are Azathioprine UNII Codes?
The UNII codes for the active ingredients in this product are:
- AZATHIOPRINE (UNII: MRK240IY2L)
- AZATHIOPRINE (UNII: MRK240IY2L) (Active Moiety)
Which are Azathioprine Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- STARCH, CORN (UNII: O8232NY3SJ)
- POVIDONE (UNII: FZ989GH94E)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- STEARIC ACID (UNII: 4ELV7Z65AP)
What is the NDC to RxNorm Crosswalk for Azathioprine?
- RxCUI: 197388 - azaTHIOprine 50 MG Oral Tablet
- RxCUI: 197388 - azathioprine 50 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Azathioprine
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.
[Learn More]
* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".