LEUPROLIDE ACETATE Detail

Drug Name(s):
LEUPROLIDE ACETATE

FDA Application No.:
NDA 074728

Active Ingredient(s):
LEUPROLIDE ACETATE

Company:
BEDFORD LABS

Original Approval or Tentative Approval Date:
August 3, 1998

Products on Application NDA 074728:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
LEUPROLIDE ACETATE	1MG/0.2ML	INJECTABLE; INJECTION	Prescription	AP

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last updated on 12-01-2008