Package 16729-486-01

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 16729-486-01
Digits Only 1672948601
Product NDC 16729-486
Product ID 16729-486_424d715c-25c3-6376-e063-6294a90a2ef4
Description

100 TABLET in 1 BOTTLE (16729-486-01)

Marketing

Marketing Status
Marketed Since 2020-08-24
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": "424d715c-25c3-6376-e063-6294a90a2ef4", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["874c7f43-a3be-4236-89cc-24c44e3c5813"], "manufacturer_name": ["Accord Healthcare Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16729-486-01)", "package_ndc": "16729-486-01", "marketing_start_date": "20200824"}], "brand_name": "Methotrexate", "product_id": "16729-486_424d715c-25c3-6376-e063-6294a90a2ef4", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "16729-486", "generic_name": "Methotrexate", "labeler_name": "Accord Healthcare Inc.", "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"}