OMEPRAZOLE Detail

Drug Name(s):
OMEPRAZOLE

FDA Application No.:
NDA 075410

Active Ingredient(s):
OMEPRAZOLE

Company:
KREMERS URBAN DEV

Products on Application NDA 075410:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
OMEPRAZOLE	10MG	CAPSULE, DELAYED REL PELLETS; ORAL	Prescription	AB

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last updated on 01-07-2009

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