Package 0703-3671-01

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 0703-3671-01
Digits Only 0703367101
Product NDC 0703-3671
Product ID 0703-3671_e81074cc-12b4-4ac9-a5bb-749188989b2c
Description

1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3671-01) / 2 mL in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2018-06-08
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": ["INTRA-ARTERIAL", "INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS"], "spl_id": "e81074cc-12b4-4ac9-a5bb-749188989b2c", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["1655956", "1655959", "1655960"], "spl_set_id": ["346ec9ce-dc98-4a55-b55e-d3af11f2d703"], "manufacturer_name": ["Teva Parenteral Medicines, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (0703-3671-01)  / 2 mL in 1 VIAL, SINGLE-DOSE", "package_ndc": "0703-3671-01", "marketing_start_date": "20180608"}], "brand_name": "Methotrexate", "product_id": "0703-3671_e81074cc-12b4-4ac9-a5bb-749188989b2c", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0703-3671", "generic_name": "Methotrexate", "labeler_name": "Teva Parenteral Medicines, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "25 mg/mL"}], "application_number": "ANDA040843", "marketing_category": "ANDA", "marketing_start_date": "20120731", "listing_expiration_date": "20261231"}