DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NEFAZODONE HYDROCHLORIDE
FDA Application No:
(ANDA) 076073
Active Ingredient(s):
NEFAZODONE HYDROCHLORIDE
Company:
WATSON LABS
Label History
Labels are not available on this site for NEFAZODONE HYDROCHLORIDE, (ANDA) 076073
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
10/29/2002
000
Tentative Approval
Other Important Information from FDA
9/16/2003
000
Approval
Other Important Information from FDA
Therapeutic Equivalents
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