Package 50090-4659-1

Brand: Hydroxychloroquine Sulfate

Generic: Hydroxychloroquine Sulfate
NDC Package

Package Facts

Identity

Package NDC 50090-4659-1
Digits Only 5009046591
Product NDC 50090-4659
Description

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

Marketing

Marketing Status
Marketed Since 2019-10-28
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": "52423747-c25c-4dc5-8cba-b734b7a7692f", "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": "60 TABLET, FILM COATED in 1 BOTTLE (50090-4659-1)", "package_ndc": "50090-4659-1", "marketing_start_date": "20191028"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (50090-4659-2)", "package_ndc": "50090-4659-2", "marketing_start_date": "20191028"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "50090-4659_52423747-c25c-4dc5-8cba-b734b7a7692f", "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": "20261231"}