Visitor Monitoring Drug Details: ROBAXIN-750
 
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Drug Details

Drug Name: ROBAXIN-750
FDA Application No: (NDA) 011011
Active Ingredient(s): METHOCARBAMOL
Company: SCHWARZ PHARMA
Original Approval or Tentative Approval Date: July 16, 1957
Chemical Type: 1 New molecular entity (NME)
Review Classification: S Standard review drug
 
Therapeutic Equivalents Label Information
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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
ROBAXIN METHOCARBAMOL500MGTABLET; ORAL Prescription Yes AA
ROBAXIN-750 METHOCARBAMOL750MGTABLET; ORAL Prescription Yes AA


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