0463-6141 NDC - PREDNISONE ()

Drug Information

Product NDC: 0463-6141

Proprietary Name: PredniSONE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: C.O. Truxton, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:2/13/2003

Package Information

No. Package Code Package Description Billing Unit
10463-6141-05500 TABLET in 1 BOTTLE, PLASTIC (0463-6141-05)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0463-6141The 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 NAMEPredniSONEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE2/13/2003This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEC.O. Truxton, 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