Package 42385-971-60

{"route": ["ORAL"], "spl_id": "5db4ef8e-532f-4bbe-94ec-489704e93be7", "openfda": {"upc": ["0342385971606"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["04d8fdbf-8829-4469-a341-8af2a2d91ccc"], "manufacturer_name": ["Laurus Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (42385-971-01)", "package_ndc": "42385-971-01", "marketing_start_date": "20230306"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (42385-971-05)", "package_ndc": "42385-971-05", "marketing_start_date": "20230306"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (42385-971-11)", "package_ndc": "42385-971-11", "marketing_start_date": "20230306"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (42385-971-60)", "package_ndc": "42385-971-60", "marketing_start_date": "20230306"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "42385-971_5db4ef8e-532f-4bbe-94ec-489704e93be7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "42385-971", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Laurus Labs Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210959", "marketing_category": "ANDA", "marketing_start_date": "20230306", "listing_expiration_date": "20261231"}