OMNIPEN-N Detail

Drug Name(s):
OMNIPEN-N

FDA Application No.:
NDA 060626

Active Ingredient(s):
AMPICILLIN SODIUM

Company:
WYETH AYERST

Products on Application NDA 060626:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
AMPICILLIN SODIUM	EQ 1GM BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none
AMPICILLIN SODIUM	EQ 250MG BASE/VIAL	INJECTABLE; INJECTION	Discontinued	none

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January 2009

OMNIPEN-N Detail

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