DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ACTOS
FDA Application No:
(NDA) 021073
Active Ingredient(s):
PIOGLITAZONE HYDROCHLORIDE
Company:
TAKEDA GLOBAL
Original Approval or Tentative Approval Date:
July 15, 1999
Chemical Type:
1 New molecular entity (NME)
Review Classification:
P Priority 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
ACTOS
PIOGLITAZONE HYDROCHLORIDE
EQ 15MG BASE
TABLET; ORAL
Prescription
No
None
ACTOS
PIOGLITAZONE HYDROCHLORIDE
EQ 30MG BASE
TABLET; ORAL
Prescription
No
None
ACTOS
PIOGLITAZONE HYDROCHLORIDE
EQ 45MG BASE
TABLET; ORAL
Prescription
Yes
None
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