DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PRELONE
FDA Application No:
(ANDA) 089081
Active Ingredient(s):
PREDNISOLONE
Company:
TEVA
Original Approval or Tentative Approval Date:
February 4, 1986
Therapeutic Equivalents
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You can see the products in the same application. The table can be sorted by clicking the header columns.
Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PRELONE
PREDNISOLONE
15MG/5ML
SYRUP; ORAL
Prescription
No
AA
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