Package 82804-136-30

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 82804-136-30
Digits Only 8280413630
Product NDC 82804-136
Product ID 82804-136_a76808f0-38a7-4b54-a4fb-3584f9058ae5
Description

30 TABLET in 1 BOTTLE (82804-136-30)

Marketing

Marketing Status
Marketed Since 2024-08-28
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": "a76808f0-38a7-4b54-a4fb-3584f9058ae5", "openfda": {"upc": ["0382804136308"], "unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["a76808f0-38a7-4b54-a4fb-3584f9058ae5"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (82804-136-30)", "package_ndc": "82804-136-30", "marketing_start_date": "20240828"}], "brand_name": "Methotrexate", "product_id": "82804-136_a76808f0-38a7-4b54-a4fb-3584f9058ae5", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "82804-136", "generic_name": "Methotrexate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA213343", "marketing_category": "ANDA", "marketing_start_date": "20200824", "listing_expiration_date": "20261231"}