Package 50742-142-01

Brand: methenamine hippurate

Generic: methenamine hippurate
NDC Package

Package Facts

Identity

Package NDC 50742-142-01
Digits Only 5074214201
Product NDC 50742-142
Product ID 50742-142_7fd02d91-96c5-46b0-a6d1-ebaef663f54c
Description

100 TABLET in 1 BOTTLE (50742-142-01)

Marketing

Marketing Status
Marketed Since 2020-12-18
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": "7fd02d91-96c5-46b0-a6d1-ebaef663f54c", "openfda": {"upc": ["0350742142019"], "unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["4412d667-63f6-427e-a5c6-376a0e1e172d"], "manufacturer_name": ["Ingenus Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (50742-142-01)", "package_ndc": "50742-142-01", "marketing_start_date": "20201218"}], "brand_name": "METHENAMINE HIPPURATE", "product_id": "50742-142_7fd02d91-96c5-46b0-a6d1-ebaef663f54c", "dosage_form": "TABLET", "product_ndc": "50742-142", "generic_name": "methenamine hippurate", "labeler_name": "Ingenus Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "METHENAMINE HIPPURATE", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1 g/1"}], "application_number": "ANDA210068", "marketing_category": "ANDA", "marketing_start_date": "20201218", "listing_expiration_date": "20261231"}