Package 51079-670-05

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 51079-670-05
Digits Only 5107967005
Product NDC 51079-670
Product ID 51079-670_3a866716-12c5-4380-e063-6394a90ae975
Description

20 BLISTER PACK in 1 CARTON (51079-670-05) / 1 TABLET in 1 BLISTER PACK (51079-670-01)

Marketing

Marketing Status
Marketed Since 1995-07-13
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": "3a866716-12c5-4380-e063-6394a90ae975", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["8df0780e-0fbd-4ab8-80b0-7a5eaa08ec0a"], "manufacturer_name": ["Mylan Institutional Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 CARTON (51079-670-05)  / 1 TABLET in 1 BLISTER PACK (51079-670-01)", "package_ndc": "51079-670-05", "marketing_start_date": "19950713"}], "brand_name": "Methotrexate", "product_id": "51079-670_3a866716-12c5-4380-e063-6394a90ae975", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "51079-670", "generic_name": "methotrexate", "labeler_name": "Mylan Institutional Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA081235", "marketing_category": "ANDA", "marketing_start_date": "19950713", "listing_expiration_date": "20261231"}