NANDROLONE DECANOATE Detail

Drug Name(s):
NANDROLONE DECANOATE

FDA Application No.:
NDA 086598

Active Ingredient(s):
NANDROLONE DECANOATE

Company:
WATSON LABS

Original Approval or Tentative Approval Date:
December 28, 1983

Products on Application NDA 086598:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NANDROLONE DECANOATE	100MG/ML	INJECTABLE; INJECTION	Prescription	none

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last updated on 12-05-2008