TAMOXIFEN CITRATE Detail

Drug Name(s):
TAMOXIFEN CITRATE

FDA Application No.:
NDA 074732

Active Ingredient(s):
TAMOXIFEN CITRATE

Company:
MYLAN

Original Approval or Tentative Approval Date:
February 19, 2003

Products on Application NDA 074732:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
TAMOXIFEN CITRATE	EQ 20MG BASE	TABLET; ORAL	Prescription	AB

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last updated on 12-01-2008

TAMOXIFEN CITRATE Detail

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