Urecholine - 51285-691-02 - (Bethanechol Chloride)

Alphabetical Index


Drug Information of Urecholine

Product NDC: 51285-691
Proprietary Name: Urecholine
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 Urecholine

Product NDC: 51285-691
Labeler Name: Teva Women's Health, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088441
Marketing Category: ANDA
Start Marketing Date: 20000401

Package Information of Urecholine

Package NDC: 51285-691-02
Package Description: 100 TABLET in 1 BOTTLE (51285-691-02)

NDC Information of Urecholine

NDC Code 51285-691-02
Proprietary Name Urecholine
Package Description 100 TABLET in 1 BOTTLE (51285-691-02)
Product NDC 51285-691
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bethanechol Chloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20000401
Marketing Category Name ANDA
Labeler Name Teva Women's Health, 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 Urecholine


General Information