Package 50268-549-15

Brand: methenamine hippurate

Generic: methenamine hippurate
NDC Package

Package Facts

Identity

Package NDC 50268-549-15
Digits Only 5026854915
Product NDC 50268-549
Description

50 BLISTER PACK in 1 CARTON (50268-549-15) / 1 TABLET in 1 BLISTER PACK (50268-549-11)

Marketing

Marketing Status
Marketed Since 2020-12-02
Brand methenamine hippurate
Generic methenamine hippurate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "0e88fdee-dba1-56cd-e063-6394a90a47c6", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["b581b655-62a4-2aa9-e053-2a95a90aa823"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (50268-549-15)  / 1 TABLET in 1 BLISTER PACK (50268-549-11)", "package_ndc": "50268-549-15", "marketing_start_date": "20201202"}], "brand_name": "Methenamine Hippurate", "product_id": "50268-549_0e88fdee-dba1-56cd-e063-6394a90a47c6", "dosage_form": "TABLET", "product_ndc": "50268-549", "generic_name": "Methenamine Hippurate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1000 mg/1"}], "application_number": "ANDA212172", "marketing_category": "ANDA", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}