DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
TANDEARIL
FDA Application No:
(NDA) 012542
Active Ingredient(s):
OXYPHENBUTAZONE
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
December 21, 1960
Chemical Type:
1 New molecular entity (NME)
Review Classification:
S Standard review drug
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
TANDEARIL
OXYPHENBUTAZONE
100MG
TABLET; ORAL
Discontinued
No
None
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