Package 50090-7307-0

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 50090-7307-0
Digits Only 5009073070
Product NDC 50090-7307
Product ID 50090-7307_e0527cfb-a490-4269-b018-1497eba45d71
Description

90 TABLET, FILM COATED in 1 BOTTLE (50090-7307-0)

Marketing

Marketing Status
Marketed Since 2024-10-14
Brand hydroxychloroquine sulfate
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (0)

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Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "e0527cfb-a490-4269-b018-1497eba45d71", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["53553ef5-5f44-4d39-ae8c-c9a632cc8416"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-7307-0)", "package_ndc": "50090-7307-0", "marketing_start_date": "20241014"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "50090-7307_e0527cfb-a490-4269-b018-1497eba45d71", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "50090-7307", "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": "20080103", "listing_expiration_date": "20261231"}