Visitor Monitoring Drug Details: WYDASE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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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
 
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
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WYDASE HYALURONIDASE1,500 UNITS/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None
WYDASE HYALURONIDASE150 UNITS/VIAL **Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons**INJECTABLE; INJECTION Discontinued No None


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