Package 68071-3765-6

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 68071-3765-6
Digits Only 6807137656
Product NDC 68071-3765
Description

60 TABLET in 1 BOTTLE (68071-3765-6)

Marketing

Marketing Status
Marketed Since 2025-01-14
Brand methotrexate
Generic methotrexate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2bae0372-8ccb-0028-e063-6294a90a889f", "openfda": {"upc": ["0368071376593"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["2b61822e-b488-5eaf-e063-6394a90a2dcd"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (68071-3765-6)", "package_ndc": "68071-3765-6", "marketing_start_date": "20250114"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68071-3765-9)", "package_ndc": "68071-3765-9", "marketing_start_date": "20250110"}], "brand_name": "Methotrexate", "product_id": "68071-3765_2bae0372-8ccb-0028-e063-6294a90a889f", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68071-3765", "generic_name": "Methotrexate", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA210454", "marketing_category": "ANDA", "marketing_start_date": "20200130", "listing_expiration_date": "20261231"}