72084-0005 NDC - LANBELLE EGF FGF AMPULE ()

Drug Information

Product NDC: 72084-0005

Proprietary Name: LANBELLE EGF FGF Ampule

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: TAMLATAMANU Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/27/2018

Package Information

No. Package Code Package Description Billing Unit
172084-0005-115 mL in 1 BOTTLE, DROPPER (72084-0005-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC72084-0005The 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 NAMELANBELLE EGF FGF AmpuleThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/27/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETAMLATAMANU Inc.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