DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE
FDA Application No:
(ANDA) 077628
Active Ingredient(s):
IBUPROFEN; PSEUDOEPHEDRINE HYDROCHLORIDE
Company:
DR REDDYS LABS LTD
Label History
Labels are not available on this site for IBUPROFEN AND PSEUDOEPHEDRINE HYDROCHLORIDE, (ANDA) 077628
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
8/14/2006
000
Approval
There are no Therapeutic Equivalents
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