Package 72578-175-01
Brand: methenamine hippurate
Generic: methenamine hippuratePackage Facts
Identity
Package NDC
72578-175-01
Digits Only
7257817501
Product NDC
72578-175
Description
100 TABLET in 1 BOTTLE (72578-175-01)
Marketing
Marketing Status
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": "d3ad1ad7-1d50-420e-9e4e-ba9283325925", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["759b3725-0934-4974-a3ac-59a20aee81c6"], "manufacturer_name": ["Viona Pharmaceuticals Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72578-175-01)", "package_ndc": "72578-175-01", "marketing_start_date": "20250312"}], "brand_name": "Methenamine hippurate", "product_id": "72578-175_d3ad1ad7-1d50-420e-9e4e-ba9283325925", "dosage_form": "TABLET", "product_ndc": "72578-175", "generic_name": "Methenamine hippurate", "labeler_name": "Viona Pharmaceuticals Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1 g/1"}], "application_number": "ANDA219661", "marketing_category": "ANDA", "marketing_start_date": "20250312", "listing_expiration_date": "20261231"}