11716-9637 NDC - LEADER DRY EYE RELIEF ()

Drug Information

Product NDC: 11716-9637

Proprietary Name: LEADER DRY EYE RELIEF

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: HANLIM PHARM. CO., LTD.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/12/2010

Package Information

No. Package Code Package Description Billing Unit
111716-9637-71 BOTTLE in 1 CARTON (11716-9637-7) / 15 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC11716-9637The 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 NAMELEADER DRY EYE RELIEFThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE7/12/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHANLIM PHARM. CO., LTD.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