Package 42291-505-01

Brand: Methotrexate

Generic: Methotrexate
NDC Package

Package Facts

Identity

Package NDC 42291-505-01
Digits Only 4229150501
Product NDC 42291-505
Product ID 42291-505_485f8485-a808-713d-e063-6394a90a771f
Description

100 TABLET in 1 BOTTLE (42291-505-01)

Marketing

Marketing Status
Discontinued 2026-02-28
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": "485f8485-a808-713d-e063-6394a90a771f", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["b0ed76b6-d9ac-c3dc-e053-2a95a90a49d4"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42291-505-01)", "package_ndc": "42291-505-01", "marketing_end_date": "20260228", "marketing_start_date": "20201005"}], "brand_name": "Methotrexate", "product_id": "42291-505_485f8485-a808-713d-e063-6394a90a771f", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "42291-505", "generic_name": "Methotrexate", "labeler_name": "AvKARE", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA210040", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20201005"}