Package 59651-182-36

{"route": ["ORAL"], "spl_id": "ce7eea99-c2b2-41c8-b577-3e7f3a29b739", "openfda": {"unii": ["3IG1E710ZN"], "rxcui": ["105585"], "spl_set_id": ["09931d44-a3f8-49dc-a3f2-b527ee4214bf"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (59651-182-01)", "package_ndc": "59651-182-01", "marketing_start_date": "20200130"}, {"sample": false, "description": "36 TABLET in 1 BOTTLE (59651-182-36)", "package_ndc": "59651-182-36", "marketing_start_date": "20200130"}], "brand_name": "Methotrexate", "product_id": "59651-182_ce7eea99-c2b2-41c8-b577-3e7f3a29b739", "dosage_form": "TABLET", "pharm_class": ["Folate Analog Metabolic Inhibitor [EPC]", "Folic Acid Metabolism Inhibitors [MoA]"], "product_ndc": "59651-182", "generic_name": "Methotrexate", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methotrexate", "active_ingredients": [{"name": "METHOTREXATE SODIUM", "strength": "2.5 mg/1"}], "application_number": "ANDA210454", "marketing_category": "ANDA", "marketing_start_date": "20200130", "listing_expiration_date": "20261231"}