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Flavoxate Hydrochloride - 54868-6326-1 - (Flavoxate hydrochloride)

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Drug Information of Flavoxate Hydrochloride

Product NDC: 54868-6326
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, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Flavoxate Hydrochloride

Product NDC: 54868-6326
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076835
Marketing Category: ANDA
Start Marketing Date: 20120104

Package Information of Flavoxate Hydrochloride

Package NDC: 54868-6326-1
Package Description: 10 TABLET, FILM COATED in 1 BOTTLE (54868-6326-1)

NDC Information of Flavoxate Hydrochloride

NDC Code 54868-6326-1
Proprietary Name Flavoxate Hydrochloride
Package Description 10 TABLET, FILM COATED in 1 BOTTLE (54868-6326-1)
Product NDC 54868-6326
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Flavoxate hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120104
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
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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