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Bethanechol Chloride - 0832-0513-50 - (Bethanechol Chloride)

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Drug Information of Bethanechol Chloride

Product NDC: 0832-0513
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: 0832-0513
Labeler Name: Upsher-Smith Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040636
Marketing Category: ANDA
Start Marketing Date: 20100124

Package Information of Bethanechol Chloride

Package NDC: 0832-0513-50
Package Description: 500 TABLET in 1 BOTTLE (0832-0513-50)

NDC Information of Bethanechol Chloride

NDC Code 0832-0513-50
Proprietary Name Bethanechol Chloride
Package Description 500 TABLET in 1 BOTTLE (0832-0513-50)
Product NDC 0832-0513
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100124
Marketing Category Name ANDA
Labeler Name Upsher-Smith Laboratories, Inc.
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