DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
LOPID
FDA Application No:
(NDA) 018422
Active Ingredient(s):
GEMFIBROZIL
Company:
PFIZER PHARMS
Original Approval or Tentative Approval Date:
December 21, 1981
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
LOPID
GEMFIBROZIL
200MG
CAPSULE; ORAL
Discontinued
No
None
LOPID
GEMFIBROZIL
300MG
CAPSULE; ORAL
Discontinued
No
None
LOPID
GEMFIBROZIL
600MG
TABLET; ORAL
Prescription
Yes
AB
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