Package 71610-701-80
Brand: hydroxychloroquine sulfate
Generic: hydroxychloroquine sulfatePackage Facts
Identity
Package NDC
71610-701-80
Digits Only
7161070180
Product NDC
71610-701
Description
180 TABLET in 1 BOTTLE (71610-701-80)
Marketing
Marketing Status
Brand
hydroxychloroquine sulfate
Generic
hydroxychloroquine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7576e78c-5a06-4d83-9f31-bca0a0cfbe87", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["beff29fe-574f-4566-99ac-53ec3b3038a7"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET in 1 BOTTLE (71610-701-53)", "package_ndc": "71610-701-53", "marketing_start_date": "20230501"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71610-701-80)", "package_ndc": "71610-701-80", "marketing_start_date": "20230414"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "71610-701_7576e78c-5a06-4d83-9f31-bca0a0cfbe87", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "71610-701", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Aphena Pharma Solutions - Tennessee, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}