Package 50090-5573-2

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 50090-5573-2
Digits Only 5009055732
Product NDC 50090-5573
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-5573-2)

Marketing

Marketing Status
Marketed Since 2021-06-29
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": "909ab143-2d20-49be-b4e8-2f4c82bade24", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["6a06ad3d-2d6c-4e51-93f5-8f782b86975b"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (50090-5573-1)", "package_ndc": "50090-5573-1", "marketing_start_date": "20210629"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-5573-2)", "package_ndc": "50090-5573-2", "marketing_start_date": "20210629"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "50090-5573_909ab143-2d20-49be-b4e8-2f4c82bade24", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-5573", "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": "ANDA040657", "marketing_category": "ANDA", "marketing_start_date": "20191001", "listing_expiration_date": "20261231"}