Visitor Monitoring Drug Details: REGLAN ODT
 
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Drug Details

Drug Name: REGLAN ODT
FDA Application No: (NDA) 021793
Active Ingredient(s): METOCLOPRAMIDE HYDROCHLORIDE
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: June 10, 2005
Chemical Type: 3 New dosage form
Review Classification: S Standard review drug
 
There are no Therapeutic Equivalents Label Information
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
REGLAN ODT METOCLOPRAMIDE HYDROCHLORIDEEQ 5MG BASETABLET, ORALLY DISINTEGRATING; ORAL Discontinued No None
REGLAN ODT METOCLOPRAMIDE HYDROCHLORIDEEQ 10MG BASETABLET, ORALLY DISINTEGRATING; ORAL Discontinued No None


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