OMEPRAZOLE Detail

Drug Name(s):
OMEPRAZOLE

FDA Application No.:
NDA 075791

Active Ingredient(s):
OMEPRAZOLE

Company:
SANDOZ

Original Approval or Tentative Approval Date:
October 23, 2002

Products on Application NDA 075791:

Active Ingredients	Strenght	Dosage Form	Marketing Status	TE Code
OMEPRAZOLE	10MG	CAPSULE, DELAYED REL PELLETS; ORAL	Tentative approval	none

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January 2009

OMEPRAZOLE Detail

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