methenamine hippurate

Generic: methenamine hippurate

Labeler: avpak
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine hippurate
Generic Name methenamine hippurate
Labeler avpak
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine hippurate 1000 mg/1

Manufacturer
AvPAK

Identifiers & Regulatory

Product NDC 50268-549
Product ID 50268-549_0e88fdee-dba1-56cd-e063-6394a90a47c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212172
Listing Expiration 2026-12-31
Marketing Start 2020-12-02

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 50268549
Hyphenated Format 50268-549

Supplemental Identifiers

RxCUI
992150
UNII
M329791L57

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 ANDA212172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (50268-549-15) / 1 TABLET in 1 BLISTER PACK (50268-549-11)
source: ndc

Packages (1)

50268-549-15 50 BLISTER PACK in 1 CARTON (50268-549-15) / 1 TABLET in 1 BLISTER PACK (50268-549-11)

Ingredients (1)

methenamine hippurate (1000 mg/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": "0e88fdee-dba1-56cd-e063-6394a90a47c6", "openfda": {"unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["b581b655-62a4-2aa9-e053-2a95a90aa823"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (50268-549-15)  / 1 TABLET in 1 BLISTER PACK (50268-549-11)", "package_ndc": "50268-549-15", "marketing_start_date": "20201202"}], "brand_name": "Methenamine Hippurate", "product_id": "50268-549_0e88fdee-dba1-56cd-e063-6394a90a47c6", "dosage_form": "TABLET", "product_ndc": "50268-549", "generic_name": "Methenamine Hippurate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Hippurate", "active_ingredients": [{"name": "METHENAMINE HIPPURATE", "strength": "1000 mg/1"}], "application_number": "ANDA212172", "marketing_category": "ANDA", "marketing_start_date": "20201202", "listing_expiration_date": "20261231"}