Package 65841-633-05

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 65841-633-05
Digits Only 6584163305
Product NDC 65841-633
Description

500 TABLET, FILM COATED in 1 BOTTLE (65841-633-05)

Marketing

Marketing Status
Marketed Since 2008-01-03
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": "63d19fd8-9254-4f19-96a7-ec9fd9b0edd1", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["1aa44bff-9a62-48b4-a520-98d7d524e3a9"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (65841-633-01)", "package_ndc": "65841-633-01", "marketing_start_date": "20080103"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (65841-633-05)", "package_ndc": "65841-633-05", "marketing_start_date": "20080103"}, {"sample": false, "description": "10 BLISTER PACK in 1 CARTON (65841-633-30)  / 10 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "65841-633-30", "marketing_start_date": "20080103"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "65841-633_63d19fd8-9254-4f19-96a7-ec9fd9b0edd1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "65841-633", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Zydus Lifesciences Limited", "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"}