Package 68382-775-60

Brand: methotrexate

Generic: methotrexate
NDC Package

Package Facts

Identity

Package NDC 68382-775-60
Digits Only 6838277560
Product NDC 68382-775
Description

36 TABLET in 1 BOTTLE (68382-775-60)

Marketing

Marketing Status
Marketed Since 2017-02-09
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": "12e61f0c-901b-4891-9a52-0cf78ebe64b6", "openfda": {"nui": ["N0000175584", "N0000000111"], "unii": ["YL5FZ2Y5U1"], "rxcui": ["105585"], "spl_set_id": ["948e0bab-6524-4b87-9853-1799d4415558"], "pharm_class_epc": ["Folate Analog Metabolic Inhibitor [EPC]"], "pharm_class_moa": ["Folic Acid Metabolism Inhibitors [MoA]"], "manufacturer_name": ["Zydus Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (68382-775-01)", "package_ndc": "68382-775-01", "marketing_start_date": "20170209"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (68382-775-05)", "package_ndc": "68382-775-05", "marketing_start_date": "20170209"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (68382-775-10)", "package_ndc": "68382-775-10", "marketing_start_date": "20170209"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE (68382-775-16)", "package_ndc": "68382-775-16", "marketing_start_date": "20170209"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (68382-775-60)", "package_ndc": "68382-775-60", "marketing_start_date": "20170209"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (68382-775-77)  / 1 TABLET in 1 BLISTER PACK", "package_ndc": "68382-775-77", "marketing_start_date": "20170209"}], "brand_name": "Methotrexate", "product_id": "68382-775_12e61f0c-901b-4891-9a52-0cf78ebe64b6", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "68382-775", "generic_name": "Methotrexate", "labeler_name": "Zydus Pharmaceuticals USA Inc.", "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"}