68258-8922 NDC - BUDESONIDE ()

Drug Information

Product NDC: 68258-8922

Proprietary Name: Budesonide

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Dispensing Solutions, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/19/2008

Package Information

No. Package Code Package Description Billing Unit
168258-8922-55 VIAL, SINGLE-DOSE in 1 POUCH (68258-8922-5) / 2 mL in 1 VIAL, SINGLE-DOSE

NDC Record

Field Name Field Value Definition
PRODUCT NDC68258-8922The 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 NAMEBudesonideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/19/2008This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDispensing Solutions, Inc.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