PANTOPRAZOLE Detail

Drug Name(s):
PANTOPRAZOLE

FDA Application No.:
NDA 077056

Active Ingredient(s):
PANTOPRAZOLE SODIUM

Company:
TEVA PHARMS

Products on Application NDA 077056:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
PANTOPRAZOLE SODIUM	40MG	TABLET, DELAYED RELEASE; ORAL	Tentative approval	none

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last updated on 12-05-2008

PANTOPRAZOLE Detail

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