Package 0143-9830-01

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 0143-9830-01
Digits Only 0143983001
Product NDC 0143-9830
Description

1 VIAL in 1 BOX (0143-9830-01) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL

Marketing

Marketing Status
Marketed Since 2017-04-25
Brand methotrexate
Generic methotrexate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRA-ARTERIAL", "INTRAMUSCULAR", "INTRATHECAL", "INTRAVENOUS"], "spl_id": "d295fa12-63ca-4760-b291-44ba56ce1b59", "openfda": {"nui": ["N0000175584", "N0000000111"], "unii": ["YL5FZ2Y5U1"], "rxcui": ["311625"], "spl_set_id": ["b080eb92-fc72-4ce6-a7ab-3f9ce2415526"], "pharm_class_epc": ["Folate Analog Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Folic Acid Metabolism Inhibitors [MoA]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX (0143-9830-01)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "0143-9830-01", "marketing_start_date": "20170425"}], "brand_name": "Methotrexate", "product_id": "0143-9830_d295fa12-63ca-4760-b291-44ba56ce1b59", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "0143-9830", "generic_name": "Methotrexate", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE", "strength": "1 g/1"}], "application_number": "ANDA040632", "marketing_category": "ANDA", "marketing_start_date": "20050906", "listing_expiration_date": "20261231"}