methenamine mandelate

Generic: methenamine mandelate

Labeler: edenbridge pharmaceuticals llc.
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name methenamine mandelate
Generic Name methenamine mandelate
Labeler edenbridge pharmaceuticals llc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

methenamine mandelate 1000 mg/1

Manufacturer
Edenbridge Pharmaceuticals LLC.

Identifiers & Regulatory

Product NDC 42799-106
Product ID 42799-106_03695bb1-8e07-4862-b517-04c39d9abee1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2027-12-31
Marketing Start 2009-12-15

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 42799106
Hyphenated Format 42799-106

Supplemental Identifiers

RxCUI
992153 992184
UPC
0342799105017 0342799106014
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 in 1 BOTTLE (42799-106-01)
source: ndc

Packages (1)

42799-106-01 100 TABLET in 1 BOTTLE (42799-106-01)

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": "03695bb1-8e07-4862-b517-04c39d9abee1", "openfda": {"upc": ["0342799105017", "0342799106014"], "unii": ["695N30CINR"], "rxcui": ["992153", "992184"], "spl_set_id": ["cc299e8a-cf9a-4dc6-b6e6-972141e59296"], "manufacturer_name": ["Edenbridge Pharmaceuticals LLC."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (42799-106-01)", "package_ndc": "42799-106-01", "marketing_start_date": "20091215"}], "brand_name": "Methenamine Mandelate", "product_id": "42799-106_03695bb1-8e07-4862-b517-04c39d9abee1", "dosage_form": "TABLET", "product_ndc": "42799-106", "generic_name": "Methenamine Mandelate", "labeler_name": "Edenbridge Pharmaceuticals 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": "20091215", "listing_expiration_date": "20271231"}