TAMOXIFEN CITRATE Detail

Drug Name(s):
TAMOXIFEN CITRATE

FDA Application No.:
NDA 076398

Active Ingredient(s):
TAMOXIFEN CITRATE

Company:
AEGIS PHARMS

Original Approval or Tentative Approval Date:
March 30, 2003

Products on Application NDA 076398:

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 11-19-2008

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