72322-1049 NDC - MYCOPHENOLIC ACID ()

Drug Information

Product NDC: 72322-1049

Proprietary Name: Mycophenolic Acid

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: AMTA LABS LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/31/2021

Package Information

No. Package Code Package Description Billing Unit
172322-1049-1120 TABLET, DELAYED RELEASE in 1 BOTTLE (72322-1049-1)
272322-1049-21000 TABLET, DELAYED RELEASE in 1 BOTTLE (72322-1049-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72322-1049The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEMycophenolic AcidThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/31/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAMTA LABS LIMITEDName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023