Healther Providers Data Logo

42254-053 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 42254-053

Proprietary Name: Omeprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Rebel Distributors Corp
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/22/2007

Package Information

No. Package Code Package Description Billing Unit
142254-053-077 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-07)EA
242254-053-1414 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-14)EA
342254-053-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-30)EA
442254-053-6060 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-60)EA
542254-053-72120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-72)EA
642254-053-9090 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42254-053-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC42254-053The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PROPRIETARY NAMEOmeprazoleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/22/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERebel Distributors CorpName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023
« Previous Code
Next Code »