LABETALOL HYDROCHLORIDE Detail

Drug Name(s):
LABETALOL HYDROCHLORIDE

FDA Application No.:
NDA 075113

Active Ingredient(s):
LABETALOL HYDROCHLORIDE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
April 29, 1999

Products on Application NDA 075113:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LABETALOL HYDROCHLORIDE	200MG	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008