Visitor Monitoring Drug Details: WYDASE
 
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Drug Details

Drug Name: WYDASE
FDA Application No: (NDA) 006343
Active Ingredient(s): HYALURONIDASE
Company: BAXTER HLTHCARE
Original Approval or Tentative Approval Date: March 22, 1950
Chemical Type: 5 New manufacturer
Review Classification: S Standard review drug
 
 
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
WYDASE HYALURONIDASE150 UNITS/MLINJECTABLE; INJECTION Discontinued No None
WYDASE HYALURONIDASE1,500 UNITS/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
WYDASE HYALURONIDASE150 UNITS/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None


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