DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
OCUFLOX
FDA Application No:
(NDA) 019921
Active Ingredient(s):
OFLOXACIN
Company:
ALLERGAN
Original Approval or Tentative Approval Date:
July 30, 1993
Chemical Type:
3 New dosage form
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
OCUFLOX
OFLOXACIN
0.3%
SOLUTION/DROPS; OPHTHALMIC
Prescription
Yes
AT
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