DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SARAFEM
FDA Application No:
(NDA) 021860
Active Ingredient(s):
FLUOXETINE HYDROCHLORIDE
Company:
WARNER CHILCOTT
Original Approval or Tentative Approval Date:
May 19, 2006
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
Label Information
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
SARAFEM
FLUOXETINE HYDROCHLORIDE
EQ 10MG BASE
TABLET; ORAL
Prescription
No
None
SARAFEM
FLUOXETINE HYDROCHLORIDE
EQ 15MG BASE
TABLET; ORAL
Prescription
No
None
SARAFEM
FLUOXETINE HYDROCHLORIDE
EQ 20MG BASE
TABLET; ORAL
Prescription
Yes
None
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