Package 76420-850-05

{"route": ["ORAL"], "spl_id": "21587ffd-a2a5-f093-e063-6394a90a6658", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["19816051-c25e-44b5-a127-e846dbd0a8d8"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-850-01)", "package_ndc": "76420-850-01", "marketing_start_date": "20240905"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (76420-850-05)", "package_ndc": "76420-850-05", "marketing_start_date": "20240905"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-850-30)", "package_ndc": "76420-850-30", "marketing_start_date": "20240905"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-850-60)", "package_ndc": "76420-850-60", "marketing_start_date": "20240905"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-850-90)", "package_ndc": "76420-850-90", "marketing_start_date": "20240905"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "76420-850_21587ffd-a2a5-f093-e063-6394a90a6658", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "76420-850", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Asclemed USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}