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Azathioprine - Medication Information

Product NDC Code 65841-602
Drug Name

Azathioprine

Type Generic
Pharm Class Nucleic Acid Synthesis Inhibitors [MoA],
Nucleosides [CS],
Purine Antimetabolite [EPC],
Purines [CS]
Active Ingredients
Azathioprine 50 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 197388
Application Number ANDA077621
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
65841-602-01 100 tablet in 1 bottle (65841-602-01)
65841-602-05 500 tablet in 1 bottle (65841-602-05)
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Spl product data elements

Usually a list of ingredients in a drug product.
Azathioprine Azathioprine AZATHIOPRINE AZATHIOPRINE CROSCARMELLOSE SODIUM LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE STARCH, CORN YELLOW ROUND ZC;59

Package label principal display panel

The content of the principal display panel of the product package, usually including the product’s name, dosage forms, and other key information about the drug product.
PACKAGE LABEL.PRINCIPAL DISPLAY PANEL NDC 65841-602-01 in bottle of 100 tablets Azathioprine Tablets USP, 50 mg 100 tablets Rx only Azathioprine Tablets, USP

Disclaimer: Do not rely on openFDA or Phanrmacy Near Me to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. Source: OpenFDA, Healthporta Drugs API