Package 70954-805-10

Brand: sovuna

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 70954-805-10
Digits Only 7095480510
Product NDC 70954-805
Product ID 70954-805_f8c163b7-15a0-424d-b53d-05fb400948bf
Description

100 TABLET, FILM COATED in 1 BOTTLE (70954-805-10)

Marketing

Marketing Status
Marketed Since 2023-09-15
Brand sovuna
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (1)

SOVUNA ndc-match (0.95)

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": "100 TABLET, FILM COATED in 1 BOTTLE (70954-805-10)", "package_ndc": "70954-805-10", "marketing_start_date": "20230915"}, {"sample": true, "description": "14 TABLET, FILM COATED in 1 BOTTLE (70954-805-20)", "package_ndc": "70954-805-20", "marketing_start_date": "20230915"}], "brand_name": "SOVUNA", "product_id": "70954-805_f8c163b7-15a0-424d-b53d-05fb400948bf", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "70954-805", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "ANI Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOVUNA", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "300 mg/1"}], "application_number": "NDA214581", "marketing_category": "NDA", "marketing_start_date": "20230915", "listing_expiration_date": "20261231"}