NDC 50090-5581 Tacrolimus
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
WHITE (C48325 - WHITE BODY)
Code Structure Chart
Product Details
What is NDC 50090-5581?
What are the uses for Tacrolimus?
Which are Tacrolimus UNII Codes?
The UNII codes for the active ingredients in this product are:
- TACROLIMUS (UNII: WM0HAQ4WNM)
- TACROLIMUS ANHYDROUS (UNII: Y5L2157C4J) (Active Moiety)
Which are Tacrolimus 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:
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- GELATIN, UNSPECIFIED (UNII: 2G86QN327L)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C RED NO. 40 (UNII: WZB9127XOA)
- SHELLAC (UNII: 46N107B71O)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POVIDONE, UNSPECIFIED (UNII: FZ989GH94E)
What is the NDC to RxNorm Crosswalk for Tacrolimus?
- RxCUI: 198377 - tacrolimus 1 MG Oral Capsule
- RxCUI: 198377 - tacrolimus 1 MG (as anhydrous tacrolimus) Oral Capsule
* Please review the disclaimer below.
Patient Education
Tacrolimus
Tacrolimus (Astagraf XL, Envarsus XR, Prograf) is used along with other medications to prevent rejection (attack of a transplanted organ by the immune system of a person receiving the organ) in people who have received a kidney transplant. Tacrolimus (Prograf) is also used along with other medications to prevent rejection in people who have received a liver, lung, or heart transplant. Tacrolimus is in a class of medications called immunosupressants. It works by decreasing the activity of the immune system to prevent it from attacking the transplanted organ.
[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".