50090-4932 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 50090-4932

Proprietary Name: Omeprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/19/2015

Package Information

No. Package Code Package Description Billing Unit
150090-4932-215 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-2)
250090-4932-360 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-3)
350090-4932-420 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-4)
450090-4932-590 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-5)EA
550090-4932-6200 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-6)
650090-4932-7180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-7)
750090-4932-87 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-8)
850090-4932-9120 CAPSULE, DELAYED RELEASE in 1 BOTTLE (50090-4932-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-4932The 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 DATE8/19/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsName 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