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BETHANECHOL CHLORIDE - 64980-162-01 - (BETHANECHOL CHLORIDE)

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Drug Information of BETHANECHOL CHLORIDE

Product NDC: 64980-162
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: 64980-162
Labeler Name: Rising Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091256
Marketing Category: ANDA
Start Marketing Date: 20100406

Package Information of BETHANECHOL CHLORIDE

Package NDC: 64980-162-01
Package Description: 100 TABLET in 1 BOTTLE (64980-162-01)

NDC Information of BETHANECHOL CHLORIDE

NDC Code 64980-162-01
Proprietary Name BETHANECHOL CHLORIDE
Package Description 100 TABLET in 1 BOTTLE (64980-162-01)
Product NDC 64980-162
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name BETHANECHOL CHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100406
Marketing Category Name ANDA
Labeler Name Rising Pharmaceuticals 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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