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Oxybutynin Chloride - 51079-628-19 - (Oxybutynin Chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 51079-628
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
Coding System: National Drug Codes(NDC)

Labeler Information of Oxybutynin Chloride

Product NDC: 51079-628
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074625
Marketing Category: ANDA
Start Marketing Date: 20110520

Package Information of Oxybutynin Chloride

Package NDC: 51079-628-19
Package Description: 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-628-19) > 1 TABLET in 1 BLISTER PACK (51079-628-17)

NDC Information of Oxybutynin Chloride

NDC Code 51079-628-19
Proprietary Name Oxybutynin Chloride
Package Description 25 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-628-19) > 1 TABLET in 1 BLISTER PACK (51079-628-17)
Product NDC 51079-628
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Oxybutynin Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110520
Marketing Category Name ANDA
Labeler Name UDL Laboratories, 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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