DRUGS THAT CAUSES A FALSE POSITIVE ON A DRUG TEST
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0-9
Drug Details
Drug Name:
PENNTUSS
FDA Application No:
(NDA) 018928
Active Ingredient(s):
CHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX
Company:
FISONS
Chemical Type:
2 New active ingredient
Review Classification:
S Standard review drug
There are no Therapeutic Equivalents
Labels are not available
Approval History and Related Documents are not available
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Drug Name
Active Ingredients
Strength
Dosage Form/Route
Marketing Status
RLD
TE Code
PENNTUSS
CHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX
EQ 4MG MALEATE/5ML; EQ 10MG BASE/5ML
SUSPENSION, EXTENDED RELEASE; ORAL
Discontinued
No
None
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