Package 42571-332-01

Brand: methenamine hippurate

Generic: methenamine hippurate
NDC Package

Package Facts

Identity

Package NDC 42571-332-01
Digits Only 4257133201
Product NDC 42571-332
Product ID 42571-332_350168e0-c68a-6cfa-e063-6294a90ab7fe
Description

100 TABLET in 1 BOTTLE (42571-332-01)

Marketing

Marketing Status
Marketed Since 2019-08-15
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": "350168e0-c68a-6cfa-e063-6294a90ab7fe", "openfda": {"upc": ["0342571332013"], "unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["e07ddd63-4725-49db-bec2-bd4f966c6e48"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42571-332-01)", "package_ndc": "42571-332-01", "marketing_start_date": "20190815"}, {"sample": false, "description": "80 TABLET in 1 CARTON (42571-332-23)", "package_ndc": "42571-332-23", "marketing_start_date": "20190815"}], "brand_name": "Methenamine Hippurate", "product_id": "42571-332_350168e0-c68a-6cfa-e063-6294a90ab7fe", "dosage_form": "TABLET", "product_ndc": "42571-332", "generic_name": "Methenamine Hippurate", "labeler_name": "Micro Labs Limited", "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": "20190815", "listing_expiration_date": "20261231"}