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bethanechol chloride - 57664-106-13 - (bethanechol chloride)

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Drug Information of bethanechol chloride

Product NDC: 57664-106
Proprietary Name: bethanechol chloride
Non Proprietary Name: bethanechol chloride
Active Ingredient(s): 50    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: 57664-106
Labeler Name: Caraco Pharmaceutical Laboratories, Ltd.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040897
Marketing Category: ANDA
Start Marketing Date: 20090430

Package Information of bethanechol chloride

Package NDC: 57664-106-13
Package Description: 500 TABLET in 1 BOTTLE (57664-106-13)

NDC Information of bethanechol chloride

NDC Code 57664-106-13
Proprietary Name bethanechol chloride
Package Description 500 TABLET in 1 BOTTLE (57664-106-13)
Product NDC 57664-106
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bethanechol chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090430
Marketing Category Name ANDA
Labeler Name Caraco Pharmaceutical Laboratories, Ltd.
Substance Name BETHANECHOL CHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]

Complete Information of bethanechol chloride


General Information