Package 72603-816-01

Brand: methenamine hippurate

Generic: methenamine hippurate
NDC Package

Package Facts

Identity

Package NDC 72603-816-01
Digits Only 7260381601
Product NDC 72603-816
Product ID 72603-816_3c9e5bea-f61d-48c3-8e05-640eccccf2ba
Description

100 TABLET in 1 BOTTLE (72603-816-01)

Marketing

Marketing Status
Marketed Since 2025-04-01
Brand methenamine hippurate
Generic methenamine hippurate
Sample Package No

Linked Drug Pages (1)

Methenamine Hippurate ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c9e5bea-f61d-48c3-8e05-640eccccf2ba", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["3c9e5bea-f61d-48c3-8e05-640eccccf2ba"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-816-01)", "package_ndc": "72603-816-01", "marketing_start_date": "20250401"}], "brand_name": "Methenamine Hippurate", "product_id": "72603-816_3c9e5bea-f61d-48c3-8e05-640eccccf2ba", "dosage_form": "TABLET", "product_ndc": "72603-816", "generic_name": "Methenamine Hippurate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1 g/1"}], "application_number": "ANDA205661", "marketing_category": "ANDA", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}