Package 60219-1544-1

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 60219-1544-1
Digits Only 6021915441
Product NDC 60219-1544
Product ID 60219-1544_9ed00eb1-8c8a-4ef0-af47-ab11bc98a9d1
Description

100 TABLET, FILM COATED in 1 BOTTLE (60219-1544-1)

Marketing

Marketing Status
Marketed Since 2018-05-17
Brand hydroxychloroquine sulfate
Generic hydroxychloroquine sulfate
Sample Package No

Linked Drug Pages (1)

Hydroxychloroquine Sulfate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "9ed00eb1-8c8a-4ef0-af47-ab11bc98a9d1", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["6a9e2fc8-bedf-46d4-9973-328dbcb18061"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (60219-1544-1)", "package_ndc": "60219-1544-1", "marketing_start_date": "20180517"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "60219-1544_9ed00eb1-8c8a-4ef0-af47-ab11bc98a9d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "60219-1544", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "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"}