DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
ACTISITE
FDA Application No:
(NDA) 050653
Active Ingredient(s):
TETRACYCLINE HYDROCHLORIDE
Company:
ON SITE
Original Approval or Tentative Approval Date:
March 25, 1994
Chemical Type:
3 New dosage form
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
ACTISITE
TETRACYCLINE HYDROCHLORIDE
12.7MG/FIBER
FIBER, EXTENDED RELEASE; PERIODONTAL
Discontinued
No
None
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