53002-3091 NDC - PREDNISONE ()

Drug Information

Product NDC: 53002-3091

Proprietary Name: Prednisone

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: RPK Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/29/2001

Package Information

No. Package Code Package Description Billing Unit
153002-3091-19 TABLET in 1 BOTTLE (53002-3091-1)
253002-3091-212 TABLET in 1 BOTTLE (53002-3091-2)
353002-3091-314 TABLET in 1 BOTTLE (53002-3091-3)
453002-3091-415 TABLET in 1 BOTTLE (53002-3091-4)
553002-3091-516 TABLET in 1 BOTTLE (53002-3091-5)
653002-3091-618 TABLET in 1 BOTTLE (53002-3091-6)
753002-3091-740 TABLET in 1 BOTTLE (53002-3091-7)
853002-3091-960 TABLET in 1 BOTTLE (53002-3091-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC53002-3091The 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 DATE8/29/2001This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMERPK Pharmaceuticals, 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