Package 67046-1524-3

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 67046-1524-3
Digits Only 6704615243
Product NDC 67046-1524
Product ID 67046-1524_2f20d43e-a477-a839-e063-6394a90ace38
Description

30 TABLET in 1 BLISTER PACK (67046-1524-3)

Marketing

Marketing Status
Marketed Since 2025-02-27
Brand methotrexate
Generic methotrexate
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": "2f20d43e-a477-a839-e063-6394a90ace38", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["2f20d43e-a4b3-a839-e063-6394a90ace38"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BLISTER PACK (67046-1524-3)", "package_ndc": "67046-1524-3", "marketing_start_date": "20250227"}], "brand_name": "Methotrexate", "product_id": "67046-1524_2f20d43e-a477-a839-e063-6394a90ace38", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "67046-1524", "generic_name": "Methotrexate", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA213343", "marketing_category": "ANDA", "marketing_start_date": "20250227", "listing_expiration_date": "20261231"}