azathioprine

Generic: azathioprine

Labeler: nucare pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azathioprine
Generic Name azathioprine
Labeler nucare pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

azathioprine 50 mg/1

Manufacturer
NuCare Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 68071-3772
Product ID 68071-3772_2b9f91b9-795a-65e7-e063-6294a90a3680
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA077621
Listing Expiration 2026-12-31
Marketing Start 2007-07-11

Pharmacologic Class

Established (EPC)
purine antimetabolite [epc]
Mechanism of Action
nucleic acid synthesis inhibitors [moa]
Chemical Structure
nucleosides [cs] purines [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713772
Hyphenated Format 68071-3772

Supplemental Identifiers

RxCUI
197388
UPC
0368071377262
UNII
MRK240IY2L
NUI
N0000000233 M0015066 N0000175712 M0018169

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name azathioprine (source: ndc)
Generic Name azathioprine (source: ndc)
Application Number ANDA077621 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 60 TABLET in 1 BOTTLE (68071-3772-6)
source: ndc

Packages (1)

68071-3772-6 60 TABLET in 1 BOTTLE (68071-3772-6)

Ingredients (1)

azathioprine (50 mg/1)

Linked Drug Pages (1)

Azathioprine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2b9f91b9-795a-65e7-e063-6294a90a3680", "openfda": {"nui": ["N0000000233", "M0015066", "N0000175712", "M0018169"], "upc": ["0368071377262"], "unii": ["MRK240IY2L"], "rxcui": ["197388"], "spl_set_id": ["2b9f91b9-7959-65e7-e063-6294a90a3680"], "pharm_class_cs": ["Nucleosides [CS]", "Purines [CS]"], "pharm_class_epc": ["Purine Antimetabolite [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3772-6)", "package_ndc": "68071-3772-6", "marketing_start_date": "20250113"}], "brand_name": "Azathioprine", "product_id": "68071-3772_2b9f91b9-795a-65e7-e063-6294a90a3680", "dosage_form": "TABLET", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "68071-3772", "generic_name": "Azathioprine", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azathioprine", "active_ingredients": [{"name": "AZATHIOPRINE", "strength": "50 mg/1"}], "application_number": "ANDA077621", "marketing_category": "ANDA", "marketing_start_date": "20070711", "listing_expiration_date": "20261231"}