Active Ingredient: DIPHENHYDRAMINE HYDROCHLORIDE; PSEUDOEPHEDRINE HYDROCHLORIDE
Proprietary Name: BENYLIN
Dosage Form; Route of Administration: SOLUTION; ORAL
Strength: 12.5MG/5ML;30MG/5ML
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N019014
Product Number: 001
Approval Date: Jun 11, 1985
Applicant Holder Full Name: PARKE DAVIS DIV WARNER LAMBERT CO
Marketing Status:
Discontinued
Patent and Exclusivity Information