Package 55154-3567-0

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 55154-3567-0
Digits Only 5515435670
Product NDC 55154-3567
Product ID 55154-3567_048ffc36-3b2f-4ce2-97dc-9dcb748b8d45
Description

10 BLISTER PACK in 1 BAG (55154-3567-0) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Marketing

Marketing Status
Marketed Since 2018-05-01
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": "048ffc36-3b2f-4ce2-97dc-9dcb748b8d45", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["e5fe2ece-40a1-49eb-818f-62ff3c3bb199"], "manufacturer_name": ["Cardinal Health 107, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "10 BLISTER PACK in 1 BAG (55154-3567-0)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "55154-3567-0", "marketing_start_date": "20180501"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "55154-3567_048ffc36-3b2f-4ce2-97dc-9dcb748b8d45", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "55154-3567", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Cardinal Health 107, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROXYCHLOROQUINE SULFATE", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210441", "marketing_category": "ANDA", "marketing_start_date": "20180501", "listing_expiration_date": "20261231"}