DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
FDA Application No:
(ANDA) 077628
Active Ingredient(s):
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Company:
DR REDDYS LABS LTD
Original Approval or Tentative Approval Date:
August 14, 2006
There are no Therapeutic Equivalents
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Approval History, Letters, Reviews and Related Documents
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
200MG; 30MG
TABLET; ORAL
OTC
No
None
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