azathioprine
Generic: azathioprine
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
azathioprine
Generic Name
azathioprine
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
azathioprine 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3544
Product ID
70518-3544_38dd6f99-80d1-9773-e063-6394a90a6f65
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208687
Listing Expiration
2026-12-31
Marketing Start
2022-09-30
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183544
Hyphenated Format
70518-3544
Supplemental Identifiers
RxCUI
UNII
NUI
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
ANDA208687 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/1
Packaging
- 100 POUCH in 1 BOX (70518-3544-0) / 1 TABLET in 1 POUCH (70518-3544-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "38dd6f99-80d1-9773-e063-6394a90a6f65", "openfda": {"nui": ["N0000000233", "M0015066", "N0000175712", "M0018169"], "unii": ["MRK240IY2L"], "rxcui": ["197388"], "spl_set_id": ["f251f372-c881-483e-8035-c6a8a6bfb4e8"], "pharm_class_cs": ["Nucleosides [CS]", "Purines [CS]"], "pharm_class_epc": ["Purine Antimetabolite [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3544-0) / 1 TABLET in 1 POUCH (70518-3544-1)", "package_ndc": "70518-3544-0", "marketing_start_date": "20220930"}], "brand_name": "Azathioprine", "product_id": "70518-3544_38dd6f99-80d1-9773-e063-6394a90a6f65", "dosage_form": "TABLET", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "70518-3544", "generic_name": "Azathioprine", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azathioprine", "active_ingredients": [{"name": "AZATHIOPRINE", "strength": "50 mg/1"}], "application_number": "ANDA208687", "marketing_category": "ANDA", "marketing_start_date": "20220930", "listing_expiration_date": "20261231"}