Package 70954-804-20
Brand: sovuna
Generic: hydroxychloroquine sulfatePackage Facts
Identity
Package NDC
70954-804-20
Digits Only
7095480420
Product NDC
70954-804
Description
100 TABLET, FILM COATED in 1 BOTTLE (70954-804-20)
Marketing
Marketing Status
Brand
sovuna
Generic
hydroxychloroquine sulfate
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "f8c163b7-15a0-424d-b53d-05fb400948bf", "openfda": {"upc": ["0370954805106", "0370954804208", "0370954804109"], "unii": ["8Q2869CNVH"], "rxcui": ["979092", "2569283", "2665282", "2665284"], "spl_set_id": ["dd441154-b196-4d4c-bc56-2e37f345ef8d"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (70954-804-10)", "package_ndc": "70954-804-10", "marketing_start_date": "20230915"}, {"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (70954-804-20)", "package_ndc": "70954-804-20", "marketing_start_date": "20230915"}, {"sample": true, "description": "14 TABLET, FILM COATED in 1 BOTTLE (70954-804-30)", "package_ndc": "70954-804-30", "marketing_start_date": "20230915"}], "brand_name": "SOVUNA", "product_id": "70954-804_f8c163b7-15a0-424d-b53d-05fb400948bf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "70954-804", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOVUNA", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "NDA214581", "marketing_category": "NDA", "marketing_start_date": "20230915", "listing_expiration_date": "20261231"}