Visitor Monitoring Drug Details: MYOTONACHOL
 
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Drug Details

Drug Name: MYOTONACHOL
FDA Application No: (ANDA) 084188
Active Ingredient(s): BETHANECHOL CHLORIDE
Company: GLENWOOD
Original Approval or Tentative Approval Date: September 24, 1975
 
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
MYOTONACHOL BETHANECHOL CHLORIDE5MGTABLET; ORAL Discontinued No None
MYOTONACHOL BETHANECHOL CHLORIDE10MGTABLET; ORAL Discontinued No None
MYOTONACHOL BETHANECHOL CHLORIDE25MGTABLET; ORAL Discontinued No None


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