70347-325 NDC - YOSPRALA ()

Drug Information

Product NDC: 70347-325

Proprietary Name: YOSPRALA

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Aralez Pharmaceuticals Us Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:9/14/2016

Package Information

No. Package Code Package Description Billing Unit
170347-325-3030 TABLET, FILM COATED in 1 BOTTLE (70347-325-30)EA
270347-325-9090 TABLET, FILM COATED in 1 BOTTLE (70347-325-90)EA

NDC Record

Field Name Field Value Definition
PRODUCT NDC70347-325The 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 NAMEYOSPRALAThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE9/14/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEAralez Pharmaceuticals Us Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023