Visitor Monitoring Drug Details: URECHOLINE
 
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Drug Details

Drug Name: URECHOLINE
FDA Application No: (NDA) 006536
Active Ingredient(s): BETHANECHOL CHLORIDE
Company: ODYSSEY PHARMS
Original Approval or Tentative Approval Date: October 12, 1948
 
There are no Therapeutic Equivalents Labels are not available
Approval History, Letters, Reviews and Related Documents
 
You can see the products in the same application. The table can be sorted by clicking the header columns.
 
Drug NameSort imageActive IngredientsStrengthDosage Form/RouteMarketing StatusRLDTE Code
URECHOLINE BETHANECHOL CHLORIDE5MG/ML **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
URECHOLINE BETHANECHOL CHLORIDE10MGTABLET; ORAL Discontinued No None
URECHOLINE BETHANECHOL CHLORIDE5MGTABLET; ORAL Discontinued No None
URECHOLINE BETHANECHOL CHLORIDE25MGTABLET; ORAL Discontinued No None
URECHOLINE BETHANECHOL CHLORIDE50MGTABLET; ORAL Discontinued No None


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