DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PATANOL
FDA Application No:
(NDA) 020688
Active Ingredient(s):
OLOPATADINE HYDROCHLORIDE
Company:
ALCON
Original Approval or Tentative Approval Date:
December 18, 1996
Chemical Type:
1 New molecular entity (NME)
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
PATANOL
OLOPATADINE HYDROCHLORIDE
EQ 0.1% BASE
SOLUTION/DROPS; OPHTHALMIC
Prescription
Yes
None
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