DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
DESMOPRESSIN ACETATE
FDA Application No:
(ANDA) 074830
Active Ingredient(s):
DESMOPRESSIN ACETATE
Company:
BAUSCH AND LOMB
Label History
Labels are not available on this site for DESMOPRESSIN ACETATE, (ANDA) 074830
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/25/1999
004
Labeling
4/28/2000
002
Microbiology
9/13/1999
001
Chemistry
1/25/1999
000
Approval
Letter
Review
Therapeutic Equivalents
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