70934-471 NDC - PREDNISONE ()

Drug Information

Product NDC: 70934-471

Proprietary Name: PREDNISONE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/9/2019

Package Information

No. Package Code Package Description Billing Unit
170934-471-1010 TABLET in 1 BOTTLE, PLASTIC (70934-471-10)EA
270934-471-1212 TABLET in 1 BOTTLE, PLASTIC (70934-471-12)EA
370934-471-1515 TABLET in 1 BOTTLE, PLASTIC (70934-471-15)EA
470934-471-1818 TABLET in 1 BOTTLE, PLASTIC (70934-471-18)
570934-471-2020 TABLET in 1 BOTTLE, PLASTIC (70934-471-20)EA
670934-471-2121 TABLET in 1 BOTTLE, PLASTIC (70934-471-21)EA
770934-471-3030 TABLET in 1 BOTTLE, PLASTIC (70934-471-30)EA
870934-471-4040 TABLET in 1 BOTTLE, PLASTIC (70934-471-40)

NDC Record

Field Name Field Value Definition
PRODUCT NDC70934-471The 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 DATE12/9/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEDenton Pharma, Inc. DBA Northwind PharmaceuticalsName 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