methenamine hippurate

Generic: methenamine hippurate

Labeler: northstar rx llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine hippurate
Generic Name methenamine hippurate
Labeler northstar rx llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine hippurate 1 g/1

Manufacturer
NorthStar Rx LLC

Identifiers & Regulatory

Product NDC 72603-816
Product ID 72603-816_3c9e5bea-f61d-48c3-8e05-640eccccf2ba
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205661
Listing Expiration 2026-12-31
Marketing Start 2025-04-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72603816
Hyphenated Format 72603-816

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 ANDA205661 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (72603-816-01)
source: ndc

Packages (1)

72603-816-01 100 TABLET in 1 BOTTLE (72603-816-01)

Ingredients (1)

methenamine hippurate (1 g/1)

Linked Drug Pages (1)

Methenamine Hippurate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3c9e5bea-f61d-48c3-8e05-640eccccf2ba", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["3c9e5bea-f61d-48c3-8e05-640eccccf2ba"], "manufacturer_name": ["NorthStar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (72603-816-01)", "package_ndc": "72603-816-01", "marketing_start_date": "20250401"}], "brand_name": "Methenamine Hippurate", "product_id": "72603-816_3c9e5bea-f61d-48c3-8e05-640eccccf2ba", "dosage_form": "TABLET", "product_ndc": "72603-816", "generic_name": "Methenamine Hippurate", "labeler_name": "NorthStar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1 g/1"}], "application_number": "ANDA205661", "marketing_category": "ANDA", "marketing_start_date": "20250401", "listing_expiration_date": "20261231"}