0597-0320 NDC - DUO FUSION ()

Drug Information

Product NDC: 0597-0320

Proprietary Name: DUO Fusion

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Boehringer Ingelheim Pharmaceuticals, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2016

Package Information

No. Package Code Package Description Billing Unit
10597-0320-3520 TABLET, CHEWABLE in 1 BOTTLE (0597-0320-35)
20597-0320-6955 TABLET, CHEWABLE in 1 BOTTLE (0597-0320-69)
30597-0320-7034 TABLET, CHEWABLE in 1 BOTTLE (0597-0320-70)

NDC Record

Field Name Field Value Definition
PRODUCT NDC0597-0320The 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 NAMEDUO FusionThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2016This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEBoehringer Ingelheim Pharmaceuticals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 5/29/2020