DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
FLAREX
FDA Application No:
(NDA) 019079
Active Ingredient(s):
FLUOROMETHOLONE ACETATE
Company:
ALCON
Original Approval or Tentative Approval Date:
February 11, 1986
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
There are no 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
FLAREX
FLUOROMETHOLONE ACETATE
0.1%
SUSPENSION/DROPS; OPHTHALMIC
Prescription
Yes
None
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