Package 70771-1058-9
Brand: methotrexate
Generic: methotrexatePackage Facts
Identity
Package NDC
70771-1058-9
Digits Only
7077110589
Product NDC
70771-1058
Description
90 TABLET in 1 BOTTLE (70771-1058-9)
Marketing
Marketing Status
Brand
methotrexate
Generic
methotrexate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "ae399908-cfb6-44dc-83da-8981f5dabbb8", "openfda": {"nui": ["N0000175584", "N0000000111"], "unii": ["YL5FZ2Y5U1"], "rxcui": ["105585"], "spl_set_id": ["59ea7b32-2b6d-4197-92c3-015936f04ebe"], "pharm_class_epc": ["Folate Analog Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Folic Acid Metabolism Inhibitors [MoA]"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1000 TABLET in 1 BOTTLE (70771-1058-0)", "package_ndc": "70771-1058-0", "marketing_start_date": "20170209"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1058-1)", "package_ndc": "70771-1058-1", "marketing_start_date": "20170209"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (70771-1058-3)", "package_ndc": "70771-1058-3", "marketing_start_date": "20170209"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (70771-1058-5)", "package_ndc": "70771-1058-5", "marketing_start_date": "20170209"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (70771-1058-7) / 1 TABLET in 1 BLISTER PACK (70771-1058-2)", "package_ndc": "70771-1058-7", "marketing_start_date": "20170209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (70771-1058-9)", "package_ndc": "70771-1058-9", "marketing_start_date": "20170209"}], "brand_name": "Methotrexate", "product_id": "70771-1058_ae399908-cfb6-44dc-83da-8981f5dabbb8", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "70771-1058", "generic_name": "Methotrexate", "labeler_name": "Zydus Lifesciences Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE", "strength": "2.5 mg/1"}], "application_number": "ANDA207812", "marketing_category": "ANDA", "marketing_start_date": "20170209", "listing_expiration_date": "20261231"}