71120-117 NDC - DURISAN ()

Drug Information

Product NDC: 71120-117

Proprietary Name: Durisan

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Sanit Technologies LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/8/2020

Package Information

No. Package Code Package Description Billing Unit
171120-117-01300 mL in 1 PACKAGE (71120-117-01)
271120-117-021000 mL in 1 PACKAGE (71120-117-02)
371120-117-033785 mL in 1 PACKAGE (71120-117-03)
471120-117-0450 mL in 1 PACKAGE (71120-117-04)
571120-117-05550 mL in 1 PACKAGE (71120-117-05)
671120-117-06250 mL in 1 PACKAGE (71120-117-06)
771120-117-071000 mL in 1 PACKAGE (71120-117-07)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71120-117The 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 NAMEDurisanThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/8/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMESanit Technologies LLCName 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