Package 70771-1919-1
Brand: methenamine hippurate
Generic: methenamine hippuratePackage Facts
Identity
Package NDC
70771-1919-1
Digits Only
7077119191
Product NDC
70771-1919
Description
100 TABLET in 1 BOTTLE (70771-1919-1)
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": "c3524692-fabc-438a-9d6e-2cca27172693", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["7e0d13d1-e564-4f3e-9054-65161eddfc57"], "manufacturer_name": ["Zydus Lifesciences Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (70771-1919-1)", "package_ndc": "70771-1919-1", "marketing_start_date": "20250312"}], "brand_name": "Methenamine hippurate", "product_id": "70771-1919_c3524692-fabc-438a-9d6e-2cca27172693", "dosage_form": "TABLET", "product_ndc": "70771-1919", "generic_name": "Methenamine hippurate", "labeler_name": "Zydus Lifesciences Limited", "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"}