DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
STARLIX
FDA Application No:
(NDA) 021204
Active Ingredient(s):
NATEGLINIDE
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
December 22, 2000
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
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
STARLIX
NATEGLINIDE
60MG
TABLET; ORAL
Prescription
No
None
STARLIX
NATEGLINIDE
120MG
TABLET; ORAL
Prescription
Yes
None
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