Visitor Monitoring Drug History: WYDASE
 
Drugs Directory of False Positives DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
 
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Label and Approval History

Drug Name: WYDASE
FDA Application No: (NDA) 006343
Active Ingredient(s): HYALURONIDASE
Company: BAXTER HLTHCARE
 
Label History
 
Labels are not available on this site for WYDASE, (NDA) 006343
 
 
 
Approval History
 
Action DateSupplement NumberSort imageApproval TypeLetters, Reviews, Labels, Patient Package Insert
7/2/2001 012Control Supplement  
4/17/2000 011Labeling Revision  
9/30/1992 010Labeling Revision  
12/1/1987 009Labeling Revision  
10/24/1985 008Practioner Draft Labeling  
11/12/1982 007Control Supplement  
3/31/1982 006Labeling Revision  
3/31/1982 005Control Supplement  
12/6/1976 004Control Supplement  
11/19/1975 003Control Supplement  
2/22/1972 001Final Printed Labeling - MarkIV  
3/22/1950 000Approval  
 
Therapeutic Equivalents
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