LABETALOL HYDROCHLORIDE Detail

Drug Name(s):
LABETALOL HYDROCHLORIDE

FDA Application No.:
NDA 075242

Active Ingredient(s):
LABETALOL HYDROCHLORIDE

Company:
MAYNE PHARMA USA

Original Approval or Tentative Approval Date:
September 16, 2001

Products on Application NDA 075242:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LABETALOL HYDROCHLORIDE	5MG/ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008