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Bethanechol Chloride - 42291-169-18 - (Bethanechol Chloride)

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Drug Information of Bethanechol Chloride

Product NDC: 42291-169
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: 42291-169
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040855
Marketing Category: ANDA
Start Marketing Date: 20100401

Package Information of Bethanechol Chloride

Package NDC: 42291-169-18
Package Description: 180 TABLET in 1 BOTTLE (42291-169-18)

NDC Information of Bethanechol Chloride

NDC Code 42291-169-18
Proprietary Name Bethanechol Chloride
Package Description 180 TABLET in 1 BOTTLE (42291-169-18)
Product NDC 42291-169
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100401
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
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


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