Package 43598-131-05

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 43598-131-05
Digits Only 4359813105
Product NDC 43598-131
Product ID 43598-131_45c22bbf-6332-4f7f-b77e-8ac613435821
Description

500 TABLET, FILM COATED in 1 BOTTLE (43598-131-05)

Marketing

Marketing Status
Marketed Since 2022-10-24
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": "45c22bbf-6332-4f7f-b77e-8ac613435821", "openfda": {"upc": ["0343598132051", "0343598133058", "0343598133010", "0343598721019"], "unii": ["8Q2869CNVH"], "rxcui": ["979092", "1119312", "2569281", "2569283"], "spl_set_id": ["452092b4-7a8f-4d19-8113-f1c2a948d3d8"], "manufacturer_name": ["Dr. Reddy's Laboratories Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (43598-131-01)", "package_ndc": "43598-131-01", "marketing_start_date": "20221024"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (43598-131-05)", "package_ndc": "43598-131-05", "marketing_start_date": "20221024"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "43598-131_45c22bbf-6332-4f7f-b77e-8ac613435821", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "43598-131", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Dr. Reddy's Laboratories Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "400 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20221024", "listing_expiration_date": "20261231"}