DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ACTIGALL
FDA Application No:
(NDA) 019594
Active Ingredient(s):
URSODIOL
Company:
WATSON PHARMS
Original Approval or Tentative Approval Date:
December 31, 1987
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority review drug
O Orphan drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
ACTIGALL
URSODIOL
150MG
CAPSULE; ORAL
Discontinued
No
None
ACTIGALL
URSODIOL
300MG
CAPSULE; ORAL
Prescription
Yes
AB
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