LABETALOL HYDROCHLORIDE Detail

Drug Name(s):
LABETALOL HYDROCHLORIDE

FDA Application No.:
NDA 074989

Active Ingredient(s):
LABETALOL HYDROCHLORIDE

Company:
TEVA

Original Approval or Tentative Approval Date:
September 29, 1998

Products on Application NDA 074989:

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