FAMOTIDINE Detail

Drug Name(s):
FAMOTIDINE

FDA Application No.:
NDA 075311

Active Ingredient(s):
FAMOTIDINE

Company:
TEVA

Original Approval or Tentative Approval Date:
April 15, 2001

Products on Application NDA 075311:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
FAMOTIDINE	20MG	TABLET; ORAL	Prescription	AB

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last updated on 12-05-2008

FAMOTIDINE Detail

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