OMEPRAZOLE Detail

Drug Name(s):
OMEPRAZOLE

FDA Application No.:
NDA 075785

Active Ingredient(s):
OMEPRAZOLE

Company:
IMPAX LABS

Products on Application NDA 075785:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
OMEPRAZOLE	20MG	CAPSULE, DELAYED REL PELLETS; ORAL	Prescription	AB

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last updated on 01-07-2009

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