Package 72162-2174-1

Brand: methotrexate

Generic: methotrexate sodium
NDC Package

Package Facts

Identity

Package NDC 72162-2174-1
Digits Only 7216221741
Product NDC 72162-2174
Product ID 72162-2174_2a3d5064-e336-459f-b0dc-28e50256b32e
Description

100 TABLET in 1 BOTTLE (72162-2174-1)

Marketing

Marketing Status
Marketed Since 2023-12-07
Brand methotrexate
Generic methotrexate sodium
Sample Package No

Linked Drug Pages (1)

Methotrexate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "2a3d5064-e336-459f-b0dc-28e50256b32e", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["c7592288-ac24-46c6-8cec-9abe23d7e81e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72162-2174-1)", "package_ndc": "72162-2174-1", "marketing_start_date": "20231207"}], "brand_name": "Methotrexate", "product_id": "72162-2174_2a3d5064-e336-459f-b0dc-28e50256b32e", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "72162-2174", "generic_name": "Methotrexate Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA201749", "marketing_category": "ANDA", "marketing_start_date": "20171110", "listing_expiration_date": "20261231"}