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Oxybutynin Chloride - 43063-145-60 - (oxybutynin chloride)

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Drug Information of Oxybutynin Chloride

Product NDC: 43063-145
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: 43063-145
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA075079
Marketing Category: ANDA
Start Marketing Date: 19971031

Package Information of Oxybutynin Chloride

Package NDC: 43063-145-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (43063-145-60)

NDC Information of Oxybutynin Chloride

NDC Code 43063-145-60
Proprietary Name Oxybutynin Chloride
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (43063-145-60)
Product NDC 43063-145
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name oxybutynin chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19971031
Marketing Category Name ANDA
Labeler Name PD-Rx 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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