Package 69238-1544-5

Brand: hydroxychloroquine sulfate

Generic: hydroxychloroquine sulfate
NDC Package

Package Facts

Identity

Package NDC 69238-1544-5
Digits Only 6923815445
Product NDC 69238-1544
Product ID 69238-1544_d3aae8a7-7df9-4771-8785-7bd6458cdfb1
Description

500 TABLET, FILM COATED in 1 BOTTLE (69238-1544-5)

Marketing

Marketing Status
Marketed Since 2019-09-17
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": "d3aae8a7-7df9-4771-8785-7bd6458cdfb1", "openfda": {"upc": ["0369238154450"], "unii": ["8Q2869CNVH"], "rxcui": ["979092"], "spl_set_id": ["7804f5d2-41a6-4523-a277-6967e984e88e"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (69238-1544-1)", "package_ndc": "69238-1544-1", "marketing_start_date": "20180517"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (69238-1544-5)", "package_ndc": "69238-1544-5", "marketing_start_date": "20190917"}], "brand_name": "Hydroxychloroquine Sulfate", "product_id": "69238-1544_d3aae8a7-7df9-4771-8785-7bd6458cdfb1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Antimalarial [EPC]", "Antirheumatic Agent [EPC]"], "product_ndc": "69238-1544", "generic_name": "Hydroxychloroquine Sulfate", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hydroxychloroquine Sulfate", "active_ingredients": [{"name": "HYDROXYCHLOROQUINE SULFATE", "strength": "200 mg/1"}], "application_number": "ANDA210577", "marketing_category": "ANDA", "marketing_start_date": "20180517", "listing_expiration_date": "20261231"}