80143-001 NDC - FLUORIDE ()

Drug Information

Product NDC: 80143-001

Proprietary Name: Fluoride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Henan Dailygreen Trade Co.,Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/24/2020

Package Information

No. Package Code Package Description Billing Unit
180143-001-0160 TABLET, CHEWABLE in 1 BOTTLE, GLASS (80143-001-01)
280143-001-0262 TABLET, CHEWABLE in 1 BOTTLE, GLASS (80143-001-02)
380143-001-03120 TABLET, CHEWABLE in 1 BOTTLE, GLASS (80143-001-03)
480143-001-0460 TABLET, CHEWABLE in 1 TUBE (80143-001-04)
580143-001-0590 TABLET, CHEWABLE in 1 TUBE (80143-001-05)
680143-001-06120 TABLET, CHEWABLE in 1 TUBE (80143-001-06)
780143-001-0730 TABLET, CHEWABLE in 1 CARTON (80143-001-07)
880143-001-0860 TABLET, CHEWABLE in 1 CARTON (80143-001-08)
980143-001-092 TABLET, CHEWABLE in 1 BAG (80143-001-09)
1080143-001-1062 TABLET, CHEWABLE in 1 BAG (80143-001-10)
1180143-001-11120 TABLET, CHEWABLE in 1 BAG (80143-001-11)
1280143-001-121000 TABLET, CHEWABLE in 1 BAG (80143-001-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC80143-001The 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 NAMEFluorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/24/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHenan Dailygreen Trade 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