Package 61703-408-41

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 61703-408-41
Digits Only 6170340841
Product NDC 61703-408
Product ID 61703-408_95b8b8da-da4e-4bba-9038-3cf65f3d5c1a
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-41) / 40 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2001-02-26
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": ["INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "95b8b8da-da4e-4bba-9038-3cf65f3d5c1a", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["1655956", "1946772"], "spl_set_id": ["0d63ba29-b692-41b4-87e8-351265c8273f"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (61703-408-41)  / 40 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "61703-408-41", "marketing_start_date": "20010226"}], "brand_name": "Methotrexate", "product_id": "61703-408_95b8b8da-da4e-4bba-9038-3cf65f3d5c1a", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "61703-408", "generic_name": "Methotrexate", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "25 mg/mL"}], "application_number": "NDA011719", "marketing_category": "NDA", "marketing_start_date": "20010226", "listing_expiration_date": "20261231"}