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) 076309
Active Ingredient(s):
NEFAZODONE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for NEFAZODONE HYDROCHLORIDE, (ANDA) 076309
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
7/7/2003
000
Tentative Approval
Other Important Information from FDA
9/16/2003
000
Approval
Other Important Information from FDA
Therapeutic Equivalents
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