methenamine hippurate

Generic: methenamine hippurate

Labeler: ingenus pharmaceuticals, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine hippurate
Generic Name methenamine hippurate
Labeler ingenus pharmaceuticals, llc
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine hippurate 1 g/1

Manufacturer
Ingenus Pharmaceuticals, LLC

Identifiers & Regulatory

Product NDC 50742-142
Product ID 50742-142_7fd02d91-96c5-46b0-a6d1-ebaef663f54c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210068
Listing Expiration 2026-12-31
Marketing Start 2020-12-18

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50742142
Hyphenated Format 50742-142

Supplemental Identifiers

RxCUI
992150
UPC
0350742142019
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 ANDA210068 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 g/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (50742-142-01)
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": "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"}