Package 71610-701-80

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package 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
Marketed Since 2023-04-14
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"}