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Bethanechol Chloride - 64679-967-01 - (Bethanechol Chloride 25 mg)

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Drug Information of Bethanechol Chloride

Product NDC: 64679-967
Proprietary Name: Bethanechol Chloride
Non Proprietary Name: Bethanechol Chloride 25 mg
Active Ingredient(s): 25    mg/1 & nbsp;   Bethanechol Chloride 25 mg
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bethanechol Chloride

Product NDC: 64679-967
Labeler Name: Wockhardt USA LLC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040534
Marketing Category: ANDA
Start Marketing Date: 20030929

Package Information of Bethanechol Chloride

Package NDC: 64679-967-01
Package Description: 100 TABLET in 1 BOTTLE (64679-967-01)

NDC Information of Bethanechol Chloride

NDC Code 64679-967-01
Proprietary Name Bethanechol Chloride
Package Description 100 TABLET in 1 BOTTLE (64679-967-01)
Product NDC 64679-967
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride 25 mg
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20030929
Marketing Category Name ANDA
Labeler Name Wockhardt USA LLC.
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


General Information