Package 50090-4659-3

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 50090-4659-3
Digits Only 5009046593
Product NDC 50090-4659
Description

12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)

Marketing

Marketing Status
Marketed Since 2020-03-17
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": "755581f8-6167-46af-991f-9cb92a16d06c", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["87076a61-ce76-475b-ac6d-c33ba617195d"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2)", "package_ndc": "50090-4659-2", "marketing_start_date": "20191028"}, {"sample": false, "description": "12 TABLET, FILM COATED in 1 BOTTLE (50090-4659-3)", "package_ndc": "50090-4659-3", "marketing_start_date": "20200317"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "50090-4659_755581f8-6167-46af-991f-9cb92a16d06c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-4659", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine Sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210577", "marketing_category": "ANDA", "marketing_start_date": "20180517", "listing_expiration_date": "20271231"}