azathioprine

Generic: azathioprine

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

azathioprine 50 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-129
Product ID 72789-129_4af728c5-ee86-3a41-e063-6394a90adfed
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074069
Listing Expiration 2027-12-31
Marketing Start 2015-02-02

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 72789129
Hyphenated Format 72789-129

Supplemental Identifiers

RxCUI
197388
UPC
0372789129303
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 ANDA074069 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 50 mg/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (72789-129-30)
source: ndc

Packages (1)

72789-129-30 30 TABLET in 1 BOTTLE, PLASTIC (72789-129-30)

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": "4af728c5-ee86-3a41-e063-6394a90adfed", "openfda": {"nui": ["N0000000233", "M0015066", "N0000175712", "M0018169"], "upc": ["0372789129303"], "unii": ["MRK240IY2L"], "rxcui": ["197388"], "spl_set_id": ["d288e484-32fc-4b46-b504-d75a0fac8663"], "pharm_class_cs": ["Nucleosides [CS]", "Purines [CS]"], "pharm_class_epc": ["Purine Antimetabolite [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-129-30)", "package_ndc": "72789-129-30", "marketing_start_date": "20201008"}], "brand_name": "AZATHIOPRINE", "product_id": "72789-129_4af728c5-ee86-3a41-e063-6394a90adfed", "dosage_form": "TABLET", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "72789-129", "generic_name": "Azathioprine", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZATHIOPRINE", "active_ingredients": [{"name": "AZATHIOPRINE", "strength": "50 mg/1"}], "application_number": "ANDA074069", "marketing_category": "ANDA", "marketing_start_date": "20150202", "listing_expiration_date": "20271231"}