Package 68084-269-01

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 68084-269-01
Digits Only 6808426901
Product NDC 68084-269
Product ID 68084-269_1ea6084a-c32f-e654-e063-6394a90ad851
Description

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-269-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-269-11)

Marketing

Marketing Status
Marketed Since 2008-09-03
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": "1ea6084a-c32f-e654-e063-6394a90ad851", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["a2d7be5a-98ee-4292-8715-46573dbe1c5b"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-269-01)  / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-269-11)", "package_ndc": "68084-269-01", "marketing_start_date": "20080903"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "68084-269_1ea6084a-c32f-e654-e063-6394a90ad851", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "68084-269", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "American Health Packaging", "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": "20080903", "listing_expiration_date": "20261231"}