NDC 72322-1049 Mycophenolic Acid
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 72322 - Amta Labs Limited
- 72322-1049 - Mycophenolic Acid
Product Characteristics
ORANGE (C48331)
OVAL (C48345)
17 MM
A121
Product Packages
NDC Code 72322-1049-1
Package Description: 120 TABLET, DELAYED RELEASE in 1 BOTTLE
NDC Code 72322-1049-2
Package Description: 1000 TABLET, DELAYED RELEASE in 1 BOTTLE
Product Details
What is NDC 72322-1049?
What are the uses for Mycophenolic Acid?
Which are Mycophenolic Acid UNII Codes?
The UNII codes for the active ingredients in this product are:
- MYCOPHENOLATE SODIUM (UNII: WX877SQI1G)
- MYCOPHENOLIC ACID (UNII: HU9DX48N0T) (Active Moiety)
Which are Mycophenolic Acid 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:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- STARCH, CORN (UNII: O8232NY3SJ)
- CROSPOVIDONE (UNII: 2S7830E561)
- FERRIC OXIDE YELLOW (UNII: EX438O2MRT)
- FD&C BLUE NO. 1--ALUMINUM LAKE (UNII: J9EQA3S2JM)
- GLYCERYL MONO AND DICAPRYLOCAPRATE (UNII: U72Q2I8C85)
- HYPROMELLOSE PHTHALATE (24% PHTHALATE, 55 CST) (UNII: 87Y6436BKR)
- LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- POVIDONE (UNII: FZ989GH94E)
- POLYVINYL ALCOHOL GRAFT POLYETHYLENE GLYCOL COPOLYMER (3:1; 45000 MW) (UNII: 23ZQ42JZZH)
- POLYVINYL ALCOHOL (UNII: 532B59J990)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FERRIC OXIDE RED (UNII: 1K09F3G675)
- HYPROMELLOSE, UNSPECIFIED (UNII: 3NXW29V3WO)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
What is the NDC to RxNorm Crosswalk for Mycophenolic Acid?
- RxCUI: 485020 - mycophenolic acid 180 MG Delayed Release Oral Tablet
- RxCUI: 485020 - mycophenolic acid (as mycophenolate sodium) 180 MG Delayed Release Oral Tablet
- RxCUI: 485023 - mycophenolic acid 360 MG Delayed Release Oral Tablet
- RxCUI: 485023 - mycophenolic acid (as mycophenolate sodium) 360 MG Delayed Release Oral Tablet
* Please review the disclaimer below.
Patient Education
Mycophenolate
Mycophenolate (CellCept) is used with other medications to help prevent transplant organ rejection (attack of the transplanted organ by the immune system of the person receiving the organ) in adults and children 3 months of age and older who have received kidney, heart, or liver transplants. Mycophenolate (Myfortic) is used with other medications to help prevent the body from rejecting kidney transplants in adults and children 5 years of age and older. Mycophenolate is in a class of medications called immunosuppressive agents. It works by weakening the body's immune system so it will not attack and reject the transplanted organ.
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* 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".