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Azathioprine - Medication Information

Product NDC Code 70771-1141
Drug Name

Azathioprine

Type Generic
Pharm Class Nucleic Acid Synthesis Inhibitors [MoA],
Nucleosides [CS],
Purine Antimetabolite [EPC],
Purines [CS]
Active Ingredients
Azathioprine 100 mg/1
Route ORAL
Dosage Form TABLET
RxCUI drug identifier 199310,
359228,
359229
Application Number ANDA077621
Labeler Name Zydus Lifesciences Limited
Packages
Package NDC Code Description
70771-1141-1 100 tablet in 1 bottle (70771-1141-1)
70771-1141-5 500 tablet in 1 bottle (70771-1141-5)
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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 ZD;11 Azathioprine Azathioprine AZATHIOPRINE AZATHIOPRINE CROSCARMELLOSE SODIUM LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE STARCH, CORN YELLOW ROUND ZD;10 Azathioprine Azathioprine AZATHIOPRINE AZATHIOPRINE CROSCARMELLOSE SODIUM LACTOSE MONOHYDRATE MAGNESIUM STEARATE POVIDONE STARCH, CORN YELLOW ROUND ZD;09

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 70771-1140-1 in bottle of 100 tablets Azathioprine Tablets USP, 75 mg 100 tablets Rx only 75 mg label 75 mg label NDC 70771-1141-1 in bottle of 100 tablets Azathioprine Tablets USP, 100 mg 100 tablets Rx only 100 mg label 100 mg label NDC 70771-1139-1 in bottle of 100 tablets Azathioprine Tablets USP, 25 mg 100 tablets Rx only 25 mg label 25 mg label

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