DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IBUPROHM COLD AND SINUS
FDA Application No:
(ANDA) 074567
Active Ingredient(s):
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Company:
OHM LABS
Original Approval or Tentative Approval Date:
April 17, 2001
There are no Therapeutic Equivalents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IBUPROHM COLD AND SINUS
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
200MG; 30MG
TABLET; ORAL
OTC
No
None
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