azathioprine
Generic: azathioprine
Labeler: ascend laboratories, llcDrug Facts
Product Profile
Brand Name
azathioprine
Generic Name
azathioprine
Labeler
ascend laboratories, llc
Dosage Form
TABLET
Routes
Active Ingredients
azathioprine 50 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
67877-493
Product ID
67877-493_7fdec2f6-c3b5-483f-8bfc-0afb292781da
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208687
Listing Expiration
2026-12-31
Marketing Start
2020-03-29
Pharmacologic Class
Established (EPC)
Mechanism of Action
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
67877493
Hyphenated Format
67877-493
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
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 TABLET in 1 BOTTLE (67877-493-01)
- 500 TABLET in 1 BOTTLE (67877-493-05)
- 1000 TABLET in 1 BOTTLE (67877-493-10)
- 10 BLISTER PACK in 1 CARTON (67877-493-38) / 10 TABLET in 1 BLISTER PACK (67877-493-33)
Packages (4)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7fdec2f6-c3b5-483f-8bfc-0afb292781da", "openfda": {"nui": ["N0000000233", "M0015066", "N0000175712", "M0018169"], "unii": ["MRK240IY2L"], "rxcui": ["197388", "199310", "359228", "359229"], "spl_set_id": ["bc6dc4bd-2121-4613-9d90-4a504010c98a"], "pharm_class_cs": ["Nucleosides [CS]", "Purines [CS]"], "pharm_class_epc": ["Purine Antimetabolite [EPC]"], "pharm_class_moa": ["Nucleic Acid Synthesis Inhibitors [MoA]"], "manufacturer_name": ["Ascend Laboratories, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (67877-493-01)", "package_ndc": "67877-493-01", "marketing_start_date": "20200329"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (67877-493-05)", "package_ndc": "67877-493-05", "marketing_start_date": "20200329"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (67877-493-10)", "package_ndc": "67877-493-10", "marketing_start_date": "20200329"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (67877-493-38) / 10 TABLET in 1 BLISTER PACK (67877-493-33)", "package_ndc": "67877-493-38", "marketing_start_date": "20200329"}], "brand_name": "Azathioprine", "product_id": "67877-493_7fdec2f6-c3b5-483f-8bfc-0afb292781da", "dosage_form": "TABLET", "pharm_class": ["Nucleic Acid Synthesis Inhibitors [MoA]", "Nucleosides [CS]", "Purine Antimetabolite [EPC]", "Purines [CS]"], "product_ndc": "67877-493", "generic_name": "Azathioprine", "labeler_name": "Ascend Laboratories, LLC", "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": "20200329", "listing_expiration_date": "20261231"}