Package 63323-123-10

Brand: methotrexate

Generic: methotrexate sodium
NDC Package

Package Facts

Identity

Package NDC 63323-123-10
Digits Only 6332312310
Product NDC 63323-123
Product ID 63323-123_880c2caa-1b11-45ce-a54e-a3733da367f0
Description

1 VIAL in 1 CARTON (63323-123-10) / 10 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2001-09-10
Brand methotrexate
Generic methotrexate sodium
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", "INTRAVENOUS"], "spl_id": "880c2caa-1b11-45ce-a54e-a3733da367f0", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["1946772"], "spl_set_id": ["b585f621-f6c9-4735-ab61-bd1b401f3df0"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-123-10)  / 10 mL in 1 VIAL", "package_ndc": "63323-123-10", "marketing_start_date": "20010910"}], "brand_name": "Methotrexate", "product_id": "63323-123_880c2caa-1b11-45ce-a54e-a3733da367f0", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "63323-123", "generic_name": "METHOTREXATE SODIUM", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "25 mg/mL"}], "application_number": "ANDA040263", "marketing_category": "ANDA", "marketing_start_date": "20010910", "listing_expiration_date": "20261231"}