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Bethanechol Chloride - 50268-114-15 - (Bethanechol Chloride)

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Drug Information of Bethanechol Chloride

Product NDC: 50268-114
Proprietary Name: Bethanechol Chloride
Non Proprietary Name: Bethanechol Chloride
Active Ingredient(s): 25    mg/1 & nbsp;   Bethanechol Chloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bethanechol Chloride

Product NDC: 50268-114
Labeler Name: AvPAK
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040855
Marketing Category: ANDA
Start Marketing Date: 20070111

Package Information of Bethanechol Chloride

Package NDC: 50268-114-15
Package Description: 50 TABLET in 1 BOX, UNIT-DOSE (50268-114-15)

NDC Information of Bethanechol Chloride

NDC Code 50268-114-15
Proprietary Name Bethanechol Chloride
Package Description 50 TABLET in 1 BOX, UNIT-DOSE (50268-114-15)
Product NDC 50268-114
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070111
Marketing Category Name ANDA
Labeler Name AvPAK
Substance Name BETHANECHOL CHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]

Complete Information of Bethanechol Chloride


General Information