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Oxybutynin Chloride - 51079-723-20 - (oxybutynin chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 51079-723
Proprietary Name: Oxybutynin Chloride
Non Proprietary Name: oxybutynin chloride
Active Ingredient(s): 10    mg/1 & nbsp;   oxybutynin chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 51079-723
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA076644
Marketing Category: ANDA
Start Marketing Date: 20110114

Package Information of Oxybutynin Chloride

Package NDC: 51079-723-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-723-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-723-01)

NDC Information of Oxybutynin Chloride

NDC Code 51079-723-20
Proprietary Name Oxybutynin Chloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-723-20) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (51079-723-01)
Product NDC 51079-723
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name TABLET, FILM COATED, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20110114
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name OXYBUTYNIN CHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]

Complete Information of Oxybutynin Chloride


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