Package 71610-506-30
Brand: hydroxychloroquine sulfate
Generic: hydroxychloroquine sulfatePackage Facts
Identity
Package NDC
71610-506-30
Digits Only
7161050630
Product NDC
71610-506
Description
30 TABLET, FILM COATED in 1 BOTTLE (71610-506-30)
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": "2027b984-d53d-41c0-914b-ff66535e0e51", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["90111c26-cd12-4a45-a25f-8d83c83c80de"], "manufacturer_name": ["Aphena Pharma Solutions - Tennessee, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71610-506-30)", "package_ndc": "71610-506-30", "marketing_start_date": "20201222"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (71610-506-53)", "package_ndc": "71610-506-53", "marketing_start_date": "20201222"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "71610-506_2027b984-d53d-41c0-914b-ff66535e0e51", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "71610-506", "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": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20080103", "listing_expiration_date": "20261231"}