Package 63629-4465-1

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 63629-4465-1
Digits Only 6362944651
Product NDC 63629-4465
Description

30 TABLET in 1 BOTTLE (63629-4465-1)

Marketing

Marketing Status
Marketed Since 2024-08-16
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": "55eb56c0-c585-4373-a3a4-9276aaeae6d6", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["2569283"], "spl_set_id": ["2c109188-d28b-4c65-8b52-819bd8547f2e"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (63629-4465-1)", "package_ndc": "63629-4465-1", "marketing_start_date": "20240816"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE (63629-4465-2)", "package_ndc": "63629-4465-2", "marketing_start_date": "20240816"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "63629-4465_55eb56c0-c585-4373-a3a4-9276aaeae6d6", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "63629-4465", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "300 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}