67544-510 NDC - OMEPRAZOLE ()

Drug Information

Product NDC: 67544-510

Proprietary Name: Omeprazole

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aphena Pharma Solutions - Tennessee, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/4/2002

Package Information

No. Package Code Package Description Billing Unit
167544-510-3030 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-30)EA
267544-510-5360 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-53)EA
367544-510-6090 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-60)EA
467544-510-70120 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-70)EA
567544-510-80180 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-80)EA
667544-510-94360 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (67544-510-94)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC67544-510The 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 DATE11/4/2002This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAphena Pharma Solutions - Tennessee, LLCName 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