Package 16571-112-10

{"route": ["ORAL"], "spl_id": "40679f36-52b2-4c4f-9a83-cc0c136077ef", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["6837f2aa-1349-4b45-a0ac-09ec914fd764"], "manufacturer_name": ["Rising Pharma Holdings, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (16571-112-01)", "package_ndc": "16571-112-01", "marketing_start_date": "20230529"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (16571-112-06)", "package_ndc": "16571-112-06", "marketing_start_date": "20230529"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (16571-112-10)", "package_ndc": "16571-112-10", "marketing_start_date": "20230529"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (16571-112-50)", "package_ndc": "16571-112-50", "marketing_start_date": "20230529"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "16571-112_40679f36-52b2-4c4f-9a83-cc0c136077ef", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "16571-112", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Rising Pharma Holdings, Inc.", "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": "20230529", "listing_expiration_date": "20261231"}