Package 83980-001-10

{"route": ["ORAL"], "spl_id": "31f4188d-1c26-4aab-aa12-354329160a39", "openfda": {"upc": ["0383980001015"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["9dfa0ff8-e8cf-47f9-847a-b86f23dc39df"], "manufacturer_name": ["Ipca Laboratories Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (83980-001-01)", "package_ndc": "83980-001-01", "marketing_start_date": "20240603"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (83980-001-05)", "package_ndc": "83980-001-05", "marketing_start_date": "20240603"}, {"sample": false, "description": "1000 TABLET, FILM COATED in 1 BOTTLE (83980-001-10)", "package_ndc": "83980-001-10", "marketing_start_date": "20240603"}, {"sample": false, "description": "10 TABLET, FILM COATED in 1 BOTTLE (83980-001-97)", "package_ndc": "83980-001-97", "marketing_start_date": "20240603"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "83980-001_31f4188d-1c26-4aab-aa12-354329160a39", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "83980-001", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Ipca Laboratories Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine Sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040766", "marketing_category": "ANDA", "marketing_start_date": "20240603", "listing_expiration_date": "20261231"}