0525-0971 NDC - ZELNORM ()

Drug Information

Product NDC: 0525-0971

Proprietary Name: ZELNORM

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Alfasigma USA, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/1/2019

Package Information

No. Package Code Package Description Billing Unit
10525-0971-101 BLISTER PACK in 1 CARTON (0525-0971-10) / 10 TABLET in 1 BLISTER PACK
20525-0971-303 BLISTER PACK in 1 CARTON (0525-0971-30) / 10 TABLET in 1 BLISTER PACK
30525-0971-606 BLISTER PACK in 1 CARTON (0525-0971-60) / 10 TABLET in 1 BLISTER PACKEA

NDC Record

Field Name Field Value Definition
PRODUCT NDC0525-0971The 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 NAMEZELNORMThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/1/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAlfasigma USA, 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