NANDROLONE PHENPROPIONATE Detail

Drug Name(s):
NANDROLONE PHENPROPIONATE

FDA Application No.:
NDA 086386

Active Ingredient(s):
NANDROLONE PHENPROPIONATE

Company:
WATSON LABS

Products on Application NDA 086386:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
NANDROLONE PHENPROPIONATE	25MG/ML	INJECTABLE; INJECTION	Discontinued	none

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last updated on 12-05-2008

NANDROLONE PHENPROPIONATE Detail

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