Package 0615-8459-39

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 0615-8459-39
Digits Only 0615845939
Product NDC 0615-8459
Product ID 0615-8459_da9a93a0-69ed-4967-b7c5-94d742615fae
Description

30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8459-39)

Marketing

Marketing Status
Marketed Since 2023-04-13
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": "da9a93a0-69ed-4967-b7c5-94d742615fae", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["83cb17e9-ce57-48aa-b92c-ac0dee92d5bc"], "manufacturer_name": ["NCS HealthCare of KY, LLC dba Vangard Labs"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8459-39)", "package_ndc": "0615-8459-39", "marketing_start_date": "20230413"}], "brand_name": "Hydroxychloroquine sulfate", "product_id": "0615-8459_da9a93a0-69ed-4967-b7c5-94d742615fae", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "0615-8459", "generic_name": "Hydroxychloroquine sulfate", "labeler_name": "NCS HealthCare of KY, LLC dba Vangard Labs", "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": "20080103", "listing_expiration_date": "20261231"}