59572-630 NDC - OTEZLA ()

Drug Information

Product NDC: 59572-630

Proprietary Name: OTEZLA

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Celgene Corporation
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/25/2014

Package Information

No. Package Code Package Description Billing Unit
159572-630-271 KIT in 1 BLISTER PACK (59572-630-27)EA
259572-630-991 KIT in 1 BLISTER PACK (59572-630-99)

NDC Record

Field Name Field Value Definition
PRODUCT NDC59572-630The 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 NAMEOTEZLAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/25/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECelgene CorporationName 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