Active Ingredient: CHLORPHENIRAMINE POLISTIREX; CODEINE POLISTIREX
Proprietary Name: PENNTUSS
Dosage Form; Route of Administration: SUSPENSION, EXTENDED RELEASE; ORAL
Strength: EQ 4MG MALEATE/5ML;EQ 10MG BASE/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018928
Product Number: 001
Approval Date: Aug 14, 1985
Applicant Holder Full Name: FISONS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information