methenamine hippurate

Generic: methenamine hippurate

Labeler: viona pharmaceuticals inc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine hippurate
Generic Name methenamine hippurate
Labeler viona pharmaceuticals inc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine hippurate 1 g/1

Manufacturer
Viona Pharmaceuticals Inc

Identifiers & Regulatory

Product NDC 72578-175
Product ID 72578-175_d3ad1ad7-1d50-420e-9e4e-ba9283325925
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA219661
Listing Expiration 2026-12-31
Marketing Start 2025-03-12

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72578175
Hyphenated Format 72578-175

Supplemental Identifiers

RxCUI
992150
UNII
M329791L57

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name methenamine hippurate (source: ndc)
Generic Name methenamine hippurate (source: ndc)
Application Number ANDA219661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72578-175-01)
source: ndc

Packages (1)

Ingredients (1)

methenamine hippurate (1 g/1)

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"}