Package 82619-131-01

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 82619-131-01
Digits Only 8261913101
Product NDC 82619-131
Description

100 TABLET in 1 BOTTLE (82619-131-01)

Marketing

Marketing Status
Marketed Since 2025-05-08
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": "40b93dff-c062-433c-e063-6294a90a6b67", "openfda": {"upc": ["0382619131017", "0382619131024", "0382619131031"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["04139607-f7c0-4fe1-a210-ffa5af347d56"], "manufacturer_name": ["Creekwood Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (82619-131-01)", "package_ndc": "82619-131-01", "marketing_start_date": "20250508"}, {"sample": false, "description": "500 TABLET in 1 BOTTLE (82619-131-02)", "package_ndc": "82619-131-02", "marketing_start_date": "20250508"}, {"sample": false, "description": "1000 TABLET in 1 BOTTLE (82619-131-03)", "package_ndc": "82619-131-03", "marketing_start_date": "20250508"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "82619-131_40b93dff-c062-433c-e063-6294a90a6b67", "dosage_form": "TABLET", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "82619-131", "generic_name": "hydroxychloroquine sulfate", "labeler_name": "Creekwood Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040150", "marketing_category": "ANDA", "marketing_start_date": "20250508", "listing_expiration_date": "20261231"}