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Flavoxate Hydrochloride - 42806-058-01 - (Flavoxate Hydrochloride)

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Drug Information of Flavoxate Hydrochloride

Product NDC: 42806-058
Proprietary Name: Flavoxate Hydrochloride
Non Proprietary Name: Flavoxate Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Flavoxate Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Flavoxate Hydrochloride

Product NDC: 42806-058
Labeler Name: Epic Pharma, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076835
Marketing Category: ANDA
Start Marketing Date: 20110221

Package Information of Flavoxate Hydrochloride

Package NDC: 42806-058-01
Package Description: 100 TABLET in 1 BOTTLE (42806-058-01)

NDC Information of Flavoxate Hydrochloride

NDC Code 42806-058-01
Proprietary Name Flavoxate Hydrochloride
Package Description 100 TABLET in 1 BOTTLE (42806-058-01)
Product NDC 42806-058
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flavoxate Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110221
Marketing Category Name ANDA
Labeler Name Epic Pharma, LLC
Substance Name FLAVOXATE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Flavoxate Hydrochloride


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