Azathioprine
Azathioprine Tablets, USP Scored Tablets PRODUCT INFORMATION Rx only
Approved
Approval ID
f251f372-c881-483e-8035-c6a8a6bfb4e8
Product Type
HUMAN PRESCRIPTION DRUG LABEL
Effective Date
Jan 15, 2024
Manufacturers
FDA
REMEDYREPACK INC.
DUNS: 829572556
Products 1
Detailed information about drug products covered under this FDA approval, including NDC codes, dosage forms, ingredients, and administration routes.
Azathioprine
PRODUCT DETAILS
NDC Product Code70518-3544
Application NumberANDA208687
Marketing CategoryC73584
Route of AdministrationORAL
Effective DateJanuary 15, 2024
Generic NameAzathioprine
INGREDIENTS (6)
POVIDONE K30Inactive
Code: U725QWY32X
Classification: IACT
AZATHIOPRINEActive
Quantity: 50 mg in 1 1
Code: MRK240IY2L
Classification: ACTIB
STARCH, CORNInactive
Code: O8232NY3SJ
Classification: IACT
MAGNESIUM STEARATEInactive
Code: 70097M6I30
Classification: IACT
LACTOSE MONOHYDRATEInactive
Code: EWQ57Q8I5X
Classification: IACT
CROSCARMELLOSE SODIUMInactive
Code: M28OL1HH48
Classification: IACT