71335-1780 NDC - PREDNISONE ()

Drug Information

Product NDC: 71335-1780

Proprietary Name: Prednisone

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Bryant Ranch Prepack
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/15/2019

Package Information

No. Package Code Package Description Billing Unit
171335-1780-042 TABLET in 1 BOTTLE (71335-1780-0)
271335-1780-130 TABLET in 1 BOTTLE (71335-1780-1)
371335-1780-278 TABLET in 1 BOTTLE (71335-1780-2)
471335-1780-336 TABLET in 1 BOTTLE (71335-1780-3)
571335-1780-421 TABLET in 1 BOTTLE (71335-1780-4)
671335-1780-515 TABLET in 1 BOTTLE (71335-1780-5)
771335-1780-6100 TABLET in 1 BOTTLE (71335-1780-6)
871335-1780-720 TABLET in 1 BOTTLE (71335-1780-7)
971335-1780-810 TABLET in 1 BOTTLE (71335-1780-8)
1071335-1780-990 TABLET in 1 BOTTLE (71335-1780-9)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71335-1780The 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 DATE11/15/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBryant Ranch PrepackName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024