71379-010 NDC - LAPCOS FRESH DAILY SUN ()

Drug Information

Product NDC: 71379-010

Proprietary Name: LAPCOS Fresh Daily Sun

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: LAP CO.,LTD
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/1/2017

Package Information

No. Package Code Package Description Billing Unit
171379-010-021 CONTAINER in 1 CARTON (71379-010-02) / 50 mL in 1 CONTAINER (71379-010-01)

NDC Record

Field Name Field Value Definition
PRODUCT NDC71379-010The 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 NAMELAPCOS Fresh Daily SunThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/1/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMELAP CO.,LTDName 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