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Methenamine Mandelate - 42799-106-99 - (Methenamine Mandelate)

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Drug Information of Methenamine Mandelate

Product NDC: 42799-106
Proprietary Name: Methenamine Mandelate
Non Proprietary Name: Methenamine Mandelate
Active Ingredient(s): 1000    mg/1 & nbsp;   Methenamine Mandelate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Methenamine Mandelate

Product NDC: 42799-106
Labeler Name: Edenbridge Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED DRUG OTHER
Start Marketing Date: 20091215

Package Information of Methenamine Mandelate

Package NDC: 42799-106-99
Package Description: 1 TABLET in 1 POUCH (42799-106-99)

NDC Information of Methenamine Mandelate

NDC Code 42799-106-99
Proprietary Name Methenamine Mandelate
Package Description 1 TABLET in 1 POUCH (42799-106-99)
Product NDC 42799-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Methenamine Mandelate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20091215
Marketing Category Name UNAPPROVED DRUG OTHER
Labeler Name Edenbridge Pharmaceuticals, LLC
Substance Name METHENAMINE MANDELATE
Strength Number 1000
Strength Unit mg/1
Pharmaceutical Classes

Complete Information of Methenamine Mandelate


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