DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FEMTRACE
FDA Application No:
(NDA) 021633
Active Ingredient(s):
ESTRADIOL ACETATE
Company:
WARNER CHILCOTT
Original Approval or Tentative Approval Date:
August 20, 2004
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
There are no 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
FEMTRACE
ESTRADIOL ACETATE
0.45MG
TABLET; ORAL
Prescription
No
None
FEMTRACE
ESTRADIOL ACETATE
0.9MG
TABLET; ORAL
Prescription
No
None
FEMTRACE
ESTRADIOL ACETATE
1.8MG
TABLET; ORAL
Prescription
Yes
None
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