Package 50090-5457-9

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 50090-5457-9
Digits Only 5009054579
Product NDC 50090-5457
Product ID 50090-5457_9a056178-22ac-4049-87ac-226d306eea2d
Description

36 TABLET in 1 BOTTLE (50090-5457-9)

Marketing

Marketing Status
Marketed Since 2021-01-29
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": "9a056178-22ac-4049-87ac-226d306eea2d", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["22e10810-16fb-4c84-bccf-972405b77ef8"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "36 TABLET in 1 BOTTLE (50090-5457-9)", "package_ndc": "50090-5457-9", "marketing_start_date": "20210129"}], "brand_name": "Methotrexate", "product_id": "50090-5457_9a056178-22ac-4049-87ac-226d306eea2d", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "50090-5457", "generic_name": "Methotrexate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA081099", "marketing_category": "ANDA", "marketing_start_date": "19901101", "listing_expiration_date": "20271231"}