58118-1429 NDC - PANTOPRAZOLE SODIUM ()

Drug Information

Product NDC: 58118-1429

Proprietary Name: Pantoprazole Sodium

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Clinical Solutions Wholesale, LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:1/17/2018

Package Information

No. Package Code Package Description Billing Unit
158118-1429-830 TABLET, DELAYED RELEASE in 1 BLISTER PACK (58118-1429-8)

NDC Record

Field Name Field Value Definition
PRODUCT NDC58118-1429The 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 NAMEPantoprazole SodiumThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE1/17/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEClinical Solutions Wholesale, 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