DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
VASOCIDIN
FDA Application No:
(ANDA) 088791
Active Ingredient(s):
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Company:
NOVARTIS
Original Approval or Tentative Approval Date:
October 5, 1984
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
VASOCIDIN
PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
0.5%; 10%
OINTMENT; OPHTHALMIC
Discontinued
No
None
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