NDC 62135-201 Methenamine Mandelate
Tablet, Film Coated Oral - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 62135 - Chartwell Rx, Llc
- 62135-201 - Methenamine Mandelate
Product Characteristics
19 MM
CE;35
Product Packages
NDC Code 62135-201-01
Package Description: 100 TABLET, FILM COATED in 1 BOTTLE
NDC Code 62135-201-12
Package Description: 120 TABLET, FILM COATED in 1 BOTTLE
Price per Unit: $1.28048 per EA
NDC Code 62135-201-60
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE
Price per Unit: $1.28048 per EA
Product Details
What is NDC 62135-201?
What are the uses for Methenamine Mandelate?
What are Methenamine Mandelate Active Ingredients?
Which are Methenamine Mandelate UNII Codes?
The UNII codes for the active ingredients in this product are:
- METHENAMINE MANDELATE (UNII: 695N30CINR)
- METHENAMINE (UNII: J50OIX95QV) (Active Moiety)
Which are Methenamine Mandelate Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- FD&C BLUE NO. 2--ALUMINUM LAKE (UNII: 4AQJ3LG584)
- MAGNESIUM STEARATE (UNII: 70097M6I30)
- MICROCRYSTALLINE CELLULOSE (UNII: OP1R32D61U)
- POLYETHYLENE GLYCOL, UNSPECIFIED (UNII: 3WJQ0SDW1A)
- POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- TALC (UNII: 7SEV7J4R1U)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Methenamine Mandelate?
- RxCUI: 992153 - methenamine mandelate 1000 MG Oral Tablet
- RxCUI: 992153 - methenamine mandelate 1 GM Oral Tablet
- RxCUI: 992184 - methenamine mandelate 500 MG Oral Tablet
* Please review the disclaimer below.
Patient Education
Methenamine
Methenamine, an antibiotic, eliminates bacteria that cause urinary tract infections. It usually is used on a long-term basis to treat chronic infections and to prevent recurrence of infections. Antibiotics will not work for colds, flu, or other viral infections. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".