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OXYBUTYNIN CHLORIDE - 60760-980-60 - (OXYBUTYNIN CHLORIDE)

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Drug Information of OXYBUTYNIN CHLORIDE

Product NDC: 60760-980
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: 60760-980
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071655
Marketing Category: ANDA
Start Marketing Date: 20130516

Package Information of OXYBUTYNIN CHLORIDE

Package NDC: 60760-980-60
Package Description: 60 TABLET in 1 BOTTLE, PLASTIC (60760-980-60)

NDC Information of OXYBUTYNIN CHLORIDE

NDC Code 60760-980-60
Proprietary Name OXYBUTYNIN CHLORIDE
Package Description 60 TABLET in 1 BOTTLE, PLASTIC (60760-980-60)
Product NDC 60760-980
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name OXYBUTYNIN CHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130516
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
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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