Package 59651-889-05

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 59651-889-05
Digits Only 5965188905
Product NDC 59651-889
Product ID 59651-889_e6f889ff-c5ba-4324-b87c-ec3ac942be2f
Description

500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59651-889-05)

Marketing

Marketing Status
Marketed Since 2025-03-07
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": "e6f889ff-c5ba-4324-b87c-ec3ac942be2f", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["e6f889ff-c5ba-4324-b87c-ec3ac942be2f"], "manufacturer_name": ["Aurobindo Pharma Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59651-889-01)", "package_ndc": "59651-889-01", "marketing_start_date": "20250307"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (59651-889-05)", "package_ndc": "59651-889-05", "marketing_start_date": "20250307"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "59651-889_e6f889ff-c5ba-4324-b87c-ec3ac942be2f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "59651-889", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Aurobindo Pharma Limited", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040274", "marketing_category": "ANDA", "marketing_start_date": "20250307", "listing_expiration_date": "20261231"}