Package 69367-615-01

Brand: salsalate

Generic: salsalate
NDC Package

Package Facts

Identity

Package NDC 69367-615-01
Digits Only 6936761501
Product NDC 69367-615
Product ID 69367-615_56747829-5049-405d-8d69-83c34d70002b
Description

100 TABLET in 1 BOTTLE (69367-615-01)

Marketing

Marketing Status
Marketed Since 2023-11-15
Brand salsalate
Generic salsalate
Sample Package No

Linked Drug Pages (1)

Salsalate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "56747829-5049-405d-8d69-83c34d70002b", "openfda": {"upc": ["0369367615013", "0369367616010"], "unii": ["V9MO595C9I"], "rxcui": ["312899", "583170"], "spl_set_id": ["24815546-658b-4b01-ac11-de7fbd0ebd16"], "manufacturer_name": ["Westminster Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (69367-615-01)", "package_ndc": "69367-615-01", "marketing_start_date": "20231115"}], "brand_name": "Salsalate", "product_id": "69367-615_56747829-5049-405d-8d69-83c34d70002b", "dosage_form": "TABLET", "product_ndc": "69367-615", "generic_name": "Salsalate", "labeler_name": "Westminster Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Salsalate", "active_ingredients": [{"name": "SALSALATE", "strength": "500 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20231115", "listing_expiration_date": "20261231"}