DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
NATEGLINIDE
FDA Application No:
(ANDA) 077467
Active Ingredient(s):
NATEGLINIDE
Company:
TEVA PHARMS
Original Approval or Tentative Approval Date:
April 26, 2007
Therapeutic Equivalents
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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
NATEGLINIDE
NATEGLINIDE
60MG
TABLET; ORAL
Tentative Approval
No
None
NATEGLINIDE
NATEGLINIDE
120MG
TABLET; ORAL
Tentative Approval
No
None
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