Visitor Monitoring Drug Details: METOCLOPRAMIDE HYDROCHLORIDE
 
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Drug Details

Drug Name: METOCLOPRAMIDE HYDROCHLORIDE
FDA Application No: (ANDA) 074478
Active Ingredient(s): METOCLOPRAMIDE HYDROCHLORIDE
Company: SANDOZ
Original Approval or Tentative Approval Date: October 5, 1995
 
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
METOCLOPRAMIDE HYDROCHLORIDE METOCLOPRAMIDE HYDROCHLORIDEEQ 5MG BASETABLET; ORAL Prescription No AB
METOCLOPRAMIDE HYDROCHLORIDE METOCLOPRAMIDE HYDROCHLORIDEEQ 10MG BASETABLET; ORAL Prescription No AB


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