73835-001 NDC - NATURALIXIR ()

Drug Information

Product NDC: 73835-001

Proprietary Name: NaturAlixir

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	North Atlantic Chemicals and Technologies LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/30/2020

No.	Package Code	Package Description
1	73835-001-02	59 mL in 1 BOTTLE (73835-001-02)
2	73835-001-04	118 mL in 1 BOTTLE (73835-001-04)
3	73835-001-08	236 mL in 1 BOTTLE (73835-001-08)
4	73835-001-10	3785 mL in 1 CONTAINER (73835-001-10)
5	73835-001-25	9463 mL in 1 CONTAINER (73835-001-25)
6	73835-001-32	946 mL in 1 BOTTLE (73835-001-32)
7	73835-001-50	18927 mL in 1 CONTAINER (73835-001-50)
8	73835-001-64	1893 mL in 1 BOTTLE (73835-001-64)

Field Name	Field Value	Definition
PRODUCT NDC	73835-001	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	NaturAlixir	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	3/30/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	North Atlantic Chemicals and Technologies LLC	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