methenamine hippurate

Generic: methenamine hippurate

Labeler: micro labs limited
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine hippurate
Generic Name methenamine hippurate
Labeler micro labs limited
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine hippurate 1000 mg/1

Manufacturer
Micro Labs Limited

Identifiers & Regulatory

Product NDC 42571-332
Product ID 42571-332_350168e0-c68a-6cfa-e063-6294a90ab7fe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA212172
Listing Expiration 2026-12-31
Marketing Start 2019-08-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42571332
Hyphenated Format 42571-332

Supplemental Identifiers

RxCUI
992150
UPC
0342571332013
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 ANDA212172 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 100 TABLET in 1 BOTTLE (42571-332-01)
  • 80 TABLET in 1 CARTON (42571-332-23)
source: ndc

Packages (2)

42571-332-01 100 TABLET in 1 BOTTLE (42571-332-01) 42571-332-23 80 TABLET in 1 CARTON (42571-332-23)

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": "350168e0-c68a-6cfa-e063-6294a90ab7fe", "openfda": {"upc": ["0342571332013"], "unii": ["M329791L57"], "rxcui": ["992150"], "spl_set_id": ["e07ddd63-4725-49db-bec2-bd4f966c6e48"], "manufacturer_name": ["Micro Labs Limited"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42571-332-01)", "package_ndc": "42571-332-01", "marketing_start_date": "20190815"}, {"sample": false, "description": "80 TABLET in 1 CARTON (42571-332-23)", "package_ndc": "42571-332-23", "marketing_start_date": "20190815"}], "brand_name": "Methenamine Hippurate", "product_id": "42571-332_350168e0-c68a-6cfa-e063-6294a90ab7fe", "dosage_form": "TABLET", "product_ndc": "42571-332", "generic_name": "Methenamine Hippurate", "labeler_name": "Micro Labs Limited", "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": "20190815", "listing_expiration_date": "20261231"}