DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
SEPTRA
FDA Application No:
(NDA) 018452
Active Ingredient(s):
SULFAMETHOXAZOLE; TRIMETHOPRIM
Company:
MONARCH PHARMS
Original Approval or Tentative Approval Date:
June 23, 1981
Chemical Type:
5 New manufacturer
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
SEPTRA
SULFAMETHOXAZOLE; TRIMETHOPRIM
80MG/ML; 16MG/ML
INJECTABLE; INJECTION
Discontinued
No
None
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