33261-117 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 33261-117

Proprietary Name: Omeprazole

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Aidarex Pharmaceuticals LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	1/21/2009

No.	Package Code	Package Description	Billing Unit
1	33261-117-02	120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-02)
2	33261-117-06	6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-06)	EA
3	33261-117-10	10 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-10)
4	33261-117-20	20 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-20)
5	33261-117-30	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-30)	EA
6	33261-117-60	60 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-60)	EA
7	33261-117-90	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (33261-117-90)	EA

Field Name	Field Value	Definition
PRODUCT NDC	33261-117	An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
PROPRIETARY NAME	Omeprazole
START MARKETING DATE	1/21/2009
LABELER NAME	Aidarex Pharmaceuticals LLC	Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 2/1/2023