Package 0006-5364-03

Brand: steglatro

Generic: ertugliflozin
NDC Package

Package Facts

Identity

Package NDC 0006-5364-03
Digits Only 0006536403
Product NDC 0006-5364
Description

30 TABLET, FILM COATED in 1 BOTTLE (0006-5364-03)

Marketing

Marketing Status
Marketed Since 2017-12-19
Brand steglatro
Generic ertugliflozin
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1616eabd-2ed5-4a98-b255-964e73b63dc8", "openfda": {"upc": ["0300065363035", "0300065364032"], "unii": ["MLU731K321"], "rxcui": ["1992810", "1992816", "1992819", "1992821"], "spl_set_id": ["e6f3e718-bb99-48f1-ab94-b9f0af05fed6"], "manufacturer_name": ["Merck Sharp & Dohme LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (0006-5364-03)", "package_ndc": "0006-5364-03", "marketing_start_date": "20171219"}, {"sample": false, "description": "90 TABLET, FILM COATED in 1 BOTTLE (0006-5364-06)", "package_ndc": "0006-5364-06", "marketing_start_date": "20171219"}, {"sample": false, "description": "500 TABLET, FILM COATED in 1 BOTTLE (0006-5364-07)", "package_ndc": "0006-5364-07", "marketing_start_date": "20171219"}, {"sample": false, "description": "2 BOTTLE in 1 CARTON (0006-5364-09)  / 7 TABLET, FILM COATED in 1 BOTTLE (0006-5364-08)", "package_ndc": "0006-5364-09", "marketing_start_date": "20171219"}], "brand_name": "STEGLATRO", "product_id": "0006-5364_1616eabd-2ed5-4a98-b255-964e73b63dc8", "dosage_form": "TABLET, FILM COATED", "product_ndc": "0006-5364", "generic_name": "ertugliflozin", "labeler_name": "Merck Sharp & Dohme LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "STEGLATRO", "active_ingredients": [{"name": "ERTUGLIFLOZIN PIDOLATE", "strength": "15 mg/1"}], "application_number": "NDA209803", "marketing_category": "NDA", "marketing_start_date": "20171219", "listing_expiration_date": "20261231"}