methenamine mandelate

Generic: methenamine mandelate

Labeler: chartwell rx, llc
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine mandelate
Generic Name methenamine mandelate
Labeler chartwell rx, llc
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

methenamine mandelate 1000 mg/1

Manufacturer
Chartwell RX, LLC

Identifiers & Regulatory

Product NDC 62135-201
Product ID 62135-201_00225fc8-eb0d-a4cc-e063-6394a90a2acb
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2021-10-01

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 62135201
Hyphenated Format 62135-201

Supplemental Identifiers

RxCUI
992153 992184
UPC
0362135201609 0362135200121 0362135200015 0362135200602 0362135201012 0362135201128
UNII
695N30CINR

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 mandelate (source: ndc)
Generic Name methenamine mandelate (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 1000 mg/1
source: ndc
Packaging
  • 100 TABLET, FILM COATED in 1 BOTTLE (62135-201-01)
  • 120 TABLET, FILM COATED in 1 BOTTLE (62135-201-12)
  • 60 TABLET, FILM COATED in 1 BOTTLE (62135-201-60)
source: ndc

Packages (3)

62135-201-01 100 TABLET, FILM COATED in 1 BOTTLE (62135-201-01) 62135-201-12 120 TABLET, FILM COATED in 1 BOTTLE (62135-201-12) 62135-201-60 60 TABLET, FILM COATED in 1 BOTTLE (62135-201-60)

Ingredients (1)

methenamine mandelate (1000 mg/1)

Linked Drug Pages (1)

Methenamine Mandelate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "00225fc8-eb0d-a4cc-e063-6394a90a2acb", "openfda": {"upc": ["0362135201609", "0362135200121", "0362135200015", "0362135200602", "0362135201012", "0362135201128"], "unii": ["695N30CINR"], "rxcui": ["992153", "992184"], "spl_set_id": ["69efa19c-64a2-41cb-a298-6e9113e57fd7"], "manufacturer_name": ["Chartwell RX, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, FILM COATED in 1 BOTTLE (62135-201-01)", "package_ndc": "62135-201-01", "marketing_start_date": "20211001"}, {"sample": false, "description": "120 TABLET, FILM COATED in 1 BOTTLE (62135-201-12)", "package_ndc": "62135-201-12", "marketing_start_date": "20211001"}, {"sample": false, "description": "60 TABLET, FILM COATED in 1 BOTTLE (62135-201-60)", "package_ndc": "62135-201-60", "marketing_start_date": "20211001"}], "brand_name": "Methenamine Mandelate", "product_id": "62135-201_00225fc8-eb0d-a4cc-e063-6394a90a2acb", "dosage_form": "TABLET, FILM COATED", "product_ndc": "62135-201", "generic_name": "Methenamine Mandelate", "labeler_name": "Chartwell RX, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Methenamine Mandelate", "active_ingredients": [{"name": "METHENAMINE MANDELATE", "strength": "1000 mg/1"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20211001", "listing_expiration_date": "20261231"}