DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
ESCITALOPRAM OXALATE
FDA Application No:
(ANDA) 078032
Active Ingredient(s):
ESCITALOPRAM OXALATE
Company:
KALI LABS
Label History
Labels are not available on this site for ESCITALOPRAM OXALATE, (ANDA) 078032
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
12/27/2006
000
Tentative Approval
Other Important Information from FDA
7/30/2007
000
Tentative Approval
Other Important Information from FDA
Therapeutic Equivalents
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