DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Label and Approval History
Drug Name:
NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
FDA Application No:
(ANDA) 077381
Active Ingredient(s):
NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
Company:
DR REDDYS LABS INC
Label History
Labels are not available on this site for NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE, (ANDA) 077381
Approval History
Action Date
Supplement Number
Approval Type
Letters, Reviews, Labels, Patient Package Insert
9/27/2006
000
Approval
Other Important Information from FDA
Patient Information Sheet
Healthcare Professional Sheet
There are no Therapeutic Equivalents
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