NDC 72322-1049 Mycophenolic Acid

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72322-1049
Proprietary Name:
Mycophenolic Acid
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Amta Labs Limited
Labeler Code:
72322
Start Marketing Date: [9]
12-31-2021
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
GREEN (C48329)
ORANGE (C48331)
Shape:
ROUND (C48348)
OVAL (C48345)
Size(s):
10 MM
17 MM
Imprint(s):
A;122
A121
Score:
1

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?

The NDC code 72322-1049 is assigned by the FDA to the product Mycophenolic Acid which is product labeled by Amta Labs Limited. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 72322-1049-1 120 tablet, delayed release in 1 bottle , 72322-1049-2 1000 tablet, delayed release in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Mycophenolic Acid?

Mycophenolate is used in combination with other medications to keep your body from attacking and rejecting your transplanted kidney. It belongs to a class of medications called immunosuppressants. It works by weakening your body's defense system (immune system) to help your body accept the new kidney as if it were your own.

Which are Mycophenolic Acid UNII Codes?

The UNII codes for the active ingredients in this product are:

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:

What is the NDC to RxNorm Crosswalk for Mycophenolic Acid?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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.
[Learn More]


* Please review the disclaimer below.

Product Footnotes

[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".