REGROTON Detail

Drug Name(s):
REGROTON

FDA Application No.:
NDA 015103

Active Ingredient(s):
CHLORTHALIDONE; RESERPINE

Company:
SANOFI AVENTIS US

Original Approval or Tentative Approval Date:
July 16, 1975

Products on Application NDA 015103:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
CHLORTHALIDONE; RESERPINE	50MG;0.25MG	TABLET; ORAL	Discontinued	none

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last updated on 11-21-2008

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