DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IBUPROFEN
FDA Application No:
(ANDA) 072169
Active Ingredient(s):
IBUPROFEN
Company:
SANDOZ
Original Approval or Tentative Approval Date:
December 11, 1987
Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IBUPROFEN
IBUPROFEN
800MG
TABLET; ORAL
Prescription
No
AB
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