Package 82009-045-05

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 82009-045-05
Digits Only 8200904505
Product NDC 82009-045
Product ID 82009-045_ddd9bc99-2f96-4baf-82a4-6fb27a3bdc07
Description

500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05)

Marketing

Marketing Status
Marketed Since 2022-09-30
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": "ddd9bc99-2f96-4baf-82a4-6fb27a3bdc07", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["81e68f23-b1bf-4561-8f02-a472631acfaf"], "manufacturer_name": ["Quallent Pharmaceuticals Health LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (82009-045-05)", "package_ndc": "82009-045-05", "marketing_start_date": "20220930"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "82009-045_ddd9bc99-2f96-4baf-82a4-6fb27a3bdc07", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "82009-045", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "Quallent Pharmaceuticals Health LLC", "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": "20220930", "listing_expiration_date": "20261231"}