Package 67046-1523-3

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 67046-1523-3
Digits Only 6704615233
Product NDC 67046-1523
Product ID 67046-1523_2eeafa6f-9d36-b46d-e063-6394a90ade46
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1523-3)

Marketing

Marketing Status
Marketed Since 2025-02-24
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": "2eeafa6f-9d36-b46d-e063-6394a90ade46", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["2eeaf562-95f9-bcef-e063-6394a90a1c19"], "manufacturer_name": ["Coupler LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1523-3)", "package_ndc": "67046-1523-3", "marketing_start_date": "20250224"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "67046-1523_2eeafa6f-9d36-b46d-e063-6394a90ade46", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "67046-1523", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Coupler LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine Sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA040766", "marketing_category": "ANDA", "marketing_start_date": "20250224", "listing_expiration_date": "20261231"}