Package 76420-643-30

{"route": ["ORAL"], "spl_id": "091085d0-27cf-a5cc-e063-6294a90a78ce", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["09109827-3053-adc8-e063-6294a90a27a6"], "manufacturer_name": ["Asclemed USA, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (76420-643-01)", "package_ndc": "76420-643-01", "marketing_start_date": "20231031"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (76420-643-30)", "package_ndc": "76420-643-30", "marketing_start_date": "20231031"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (76420-643-60)", "package_ndc": "76420-643-60", "marketing_start_date": "20231031"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (76420-643-90)", "package_ndc": "76420-643-90", "marketing_start_date": "20231031"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "76420-643_091085d0-27cf-a5cc-e063-6294a90a78ce", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "76420-643", "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": "ANDA210959", "marketing_category": "ANDA", "marketing_start_date": "20190905", "listing_expiration_date": "20261231"}