80371-103 NDC - BIOLUSTRE LIQUID DISINFECTANT ()

Drug Information

Product NDC: 80371-103

Proprietary Name: Biolustre Liquid Disinfectant

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	KOYUNCU BILISIM TEKNOLOJILERI SANAYI VE TICARET LIMITED SIRKETI
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	8/31/2020

No.	Package Code	Package Description
1	80371-103-01	50 mL in 1 BOTTLE, PLASTIC (80371-103-01)
2	80371-103-02	100 mL in 1 BOTTLE, PLASTIC (80371-103-02)
3	80371-103-03	250 mL in 1 BOTTLE, PLASTIC (80371-103-03)
4	80371-103-04	500 mL in 1 BOTTLE, PLASTIC (80371-103-04)
5	80371-103-05	1000 mL in 1 BOTTLE, PUMP (80371-103-05)
6	80371-103-06	5000 mL in 1 BOTTLE, PLASTIC (80371-103-06)

Field Name	Field Value	Definition
PRODUCT NDC	80371-103	The 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 NAME	Biolustre Liquid Disinfectant	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE	8/31/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	KOYUNCU BILISIM TEKNOLOJILERI SANAYI VE TICARET LIMITED SIRKETI	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