Package 51285-369-01
Brand: trexall
Generic: methotrexatePackage Facts
Identity
Package NDC
51285-369-01
Digits Only
5128536901
Product NDC
51285-369
Description
30 TABLET, FILM COATED in 1 BOTTLE (51285-369-01)
Marketing
Marketing Status
Brand
trexall
Generic
methotrexate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "6743bd6d-9c6b-4f43-b444-8faa4b5d5221", "openfda": {"upc": ["0351285367013", "0351285366016", "0351285369017"], "unii": ["3IG1E710ZN"], "rxcui": ["105586", "283510", "283511", "283671", "284592", "284593", "284594", "284595"], "spl_set_id": ["e942f8db-510f-44d6-acb5-b822196f5e8c"], "manufacturer_name": ["Teva Women's Health, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (51285-369-01)", "package_ndc": "51285-369-01", "marketing_start_date": "20010503"}], "brand_name": "Trexall", "product_id": "51285-369_6743bd6d-9c6b-4f43-b444-8faa4b5d5221", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "51285-369", "generic_name": "Methotrexate", "labeler_name": "Teva Women's Health, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Trexall", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "15 mg/1"}], "application_number": "ANDA040385", "marketing_category": "ANDA", "marketing_start_date": "20010503", "listing_expiration_date": "20261231"}