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Bethanechol Chloride - 0615-2557-39 - (Bethanechol Chloride)

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Drug Information of Bethanechol Chloride

Product NDC: 0615-2557
Proprietary Name: Bethanechol Chloride
Non Proprietary Name: Bethanechol Chloride
Active Ingredient(s): 10    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: 0615-2557
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040533
Marketing Category: ANDA
Start Marketing Date: 20030929

Package Information of Bethanechol Chloride

Package NDC: 0615-2557-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-2557-39)

NDC Information of Bethanechol Chloride

NDC Code 0615-2557-39
Proprietary Name Bethanechol Chloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-2557-39)
Product NDC 0615-2557
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030929
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name BETHANECHOL CHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Cholinergic Muscarinic Agonist [EPC],Cholinergic Muscarinic Agonists [MoA]

Complete Information of Bethanechol Chloride


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