DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
JANUVIA
FDA Application No:
(NDA) 021995
Active Ingredient(s):
SITAGLIPTIN PHOSPHATE
Company:
MERCK CO INC
Original Approval or Tentative Approval Date:
October 16, 2006
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
JANUVIA
SITAGLIPTIN PHOSPHATE
EQ 25MG BASE
TABLET; ORAL
Prescription
No
None
JANUVIA
SITAGLIPTIN PHOSPHATE
EQ 50MG BASE
TABLET; ORAL
Prescription
No
None
JANUVIA
SITAGLIPTIN PHOSPHATE
EQ 100MG BASE
TABLET; ORAL
Prescription
Yes
None
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