Package 0904-7046-61

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 0904-7046-61
Digits Only 0904704661
Product NDC 0904-7046
Product ID 0904-7046_a0a69116-862a-4dfa-820f-33e95343edfe
Description

100 BLISTER PACK in 1 CARTON (0904-7046-61) / 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": "a0a69116-862a-4dfa-820f-33e95343edfe", "openfda": {"unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["ebe00e35-ed3d-40f4-9a93-a37b0da01ddb"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7046-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7046-06", "marketing_start_date": "20180501"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7046-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7046-61", "marketing_start_date": "20180501"}], "brand_name": "HYDROXYCHLOROQUINE SULFATE", "product_id": "0904-7046_a0a69116-862a-4dfa-820f-33e95343edfe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "0904-7046", "generic_name": "HYDROXYCHLOROQUINE SULFATE", "labeler_name": "Major Pharmaceuticals", "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"}