azathioprine

Generic: azathioprine

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

Drug Facts

Product Profile

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

azathioprine 50 mg/1

Manufacturer
Glenmark Pharmaceuticals, Inc

Identifiers & Regulatory

Product NDC 68462-502
Product ID 68462-502_26e47a7e-a3b4-036a-e063-6394a90ae208
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075252
Listing Expiration 2026-12-31
Marketing Start 1999-08-01

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 68462502
Hyphenated Format 68462-502

Supplemental Identifiers

RxCUI
197388
UPC
0368462502013
UNII
MRK240IY2L
NUI
N0000000233 M0015066 N0000175712 M0018169

Packaging Origin

Original Packager
true

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 ANDA075252 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (68462-502-01)
source: ndc

Packages (1)

68462-502-01 100 TABLET in 1 BOTTLE (68462-502-01)

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": "26e47a7e-a3b4-036a-e063-6394a90ae208", "openfda": {"nui": ["N0000000233", "M0015066", "N0000175712", "M0018169"], "upc": ["0368462502013"], "unii": ["MRK240IY2L"], "rxcui": ["197388"], "spl_set_id": ["ceab8e8b-d022-4d0c-a552-cc5782446248"], "pharm_class_cs": ["Nucleosides [CS]", "Purines [CS]"], "pharm_class_epc": ["Purine Antimetabolite [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Glenmark Pharmaceuticals, Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68462-502-01)", "package_ndc": "68462-502-01", "marketing_start_date": "19990801"}], "brand_name": "Azathioprine", "product_id": "68462-502_26e47a7e-a3b4-036a-e063-6394a90ae208", "dosage_form": "TABLET", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "68462-502", "generic_name": "Azathioprine", "labeler_name": "Glenmark Pharmaceuticals, Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azathioprine", "active_ingredients": [{"name": "AZATHIOPRINE", "strength": "50 mg/1"}], "application_number": "ANDA075252", "marketing_category": "ANDA", "marketing_start_date": "19990801", "listing_expiration_date": "20261231"}