DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NEFAZODONE HYDROCHLORIDE
FDA Application No:
(ANDA) 075763
Active Ingredient(s):
NEFAZODONE HYDROCHLORIDE
Company:
IVAX PHARMS
Original Approval or Tentative Approval Date:
September 16, 2003
Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
NEFAZODONE HYDROCHLORIDE
NEFAZODONE HYDROCHLORIDE
50MG
TABLET; ORAL
Prescription
No
AB
NEFAZODONE HYDROCHLORIDE
NEFAZODONE HYDROCHLORIDE
100MG
TABLET; ORAL
Prescription
No
AB
NEFAZODONE HYDROCHLORIDE
NEFAZODONE HYDROCHLORIDE
150MG
TABLET; ORAL
Prescription
No
AB
NEFAZODONE HYDROCHLORIDE
NEFAZODONE HYDROCHLORIDE
200MG
TABLET; ORAL
Prescription
No
AB
NEFAZODONE HYDROCHLORIDE
NEFAZODONE HYDROCHLORIDE
250MG
TABLET; ORAL
Prescription
No
AB
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