DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
GANTRISIN
FDA Application No:
(NDA) 009182
Active Ingredient(s):
SULFISOXAZOLE ACETYL
Company:
ROCHE
Original Approval or Tentative Approval Date:
December 4, 1953
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
GANTRISIN
SULFISOXAZOLE ACETYL
EQ 500MG BASE/5ML
SYRUP; ORAL
Discontinued
No
None
GANTRISIN PEDIATRIC
SULFISOXAZOLE ACETYL
EQ 500MG BASE/5ML
SUSPENSION; ORAL
Prescription
Yes
None
LIPO GANTRISIN
SULFISOXAZOLE ACETYL
EQ 1GM BASE/5ML
EMULSION; ORAL
Discontinued
No
None
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