BENADRYL Detail

Drug Name(s):
BENADRYL

FDA Application No.:
NDA 006146

Active Ingredient(s):
DIPHENHYDRAMINE HYDROCHLORIDE

Company:
PARKE DAVIS

Original Approval or Tentative Approval Date:
August 9, 1984

Products on Application NDA 006146:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
DIPHENHYDRAMINE HYDROCHLORIDE	50MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 11-21-2008

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