OMEPRAZOLE Detail

Drug Name(s):
OMEPRAZOLE

FDA Application No.:
NDA 075757

Active Ingredient(s):
OMEPRAZOLE

Company:
LEK PHARMS

Original Approval or Tentative Approval Date:
January 27, 2003

Products on Application NDA 075757:

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

Recall Notices

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January 2009

OMEPRAZOLE Detail

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