0642-7471 NDC - TYBLUME ()

Drug Information

Product NDC: 0642-7471

Proprietary Name: Tyblume

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Exeltis USA, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/26/2020

Package Information

No. Package Code Package Description Billing Unit
10642-7471-011 BLISTER PACK in 1 BOX (0642-7471-01) / 1 KIT in 1 BLISTER PACK
20642-7471-033 BLISTER PACK in 1 BOX (0642-7471-03) / 1 KIT in 1 BLISTER PACK
30642-7471-066 BLISTER PACK in 1 BOX (0642-7471-06) / 1 KIT in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC0642-7471The 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 NAMETyblumeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/26/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEExeltis 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