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Oxybutynin Chloride - 62175-270-43 - (Oxybutynin Chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 62175-270
Proprietary Name: Oxybutynin Chloride
Non Proprietary Name: Oxybutynin Chloride
Active Ingredient(s): 5    mg/1 & nbsp;   Oxybutynin Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 62175-270
Labeler Name: Kremers Urban Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078503
Marketing Category: ANDA
Start Marketing Date: 20090301

Package Information of Oxybutynin Chloride

Package NDC: 62175-270-43
Package Description: 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-270-43)

NDC Information of Oxybutynin Chloride

NDC Code 62175-270-43
Proprietary Name Oxybutynin Chloride
Package Description 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (62175-270-43)
Product NDC 62175-270
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxybutynin Chloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20090301
Marketing Category Name ANDA
Labeler Name Kremers Urban Pharmaceuticals Inc.
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Oxybutynin Chloride


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