Package 57664-761-13

{"route": ["ORAL"], "spl_id": "cb7adb60-886b-4415-9b04-b6d37712bbe0", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["6e72fe06-7995-3fd7-e053-2a91aa0a54db"], "manufacturer_name": ["Sun Pharmaceutical Industries, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET in 1 BOTTLE (57664-761-13)", "package_ndc": "57664-761-13", "marketing_start_date": "20180618"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (57664-761-88)", "package_ndc": "57664-761-88", "marketing_start_date": "20180618"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "57664-761_cb7adb60-886b-4415-9b04-b6d37712bbe0", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "57664-761", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Sun Pharmaceutical Industries, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA201691", "marketing_category": "ANDA", "marketing_start_date": "20180618", "listing_expiration_date": "20261231"}