73689-101 NDC - FAIRFIELD HEALTH PRODUCTS EXTRA STRENGTH ()

Drug Information

Product NDC: 73689-101

Proprietary Name: FAIRFIELD HEALTH PRODUCTS EXTRA STRENGTH

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Fairfield Health Products Llc
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	3/12/2020

No.	Package Code	Package Description	Billing Unit
1	73689-101-02	25 PACKET in 1 BOX (73689-101-02) / 2 TABLET, FILM COATED in 1 PACKET (73689-101-01)

Field Name	Field Value	Definition
PRODUCT NDC	73689-101	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	FAIRFIELD HEALTH PRODUCTS EXTRA STRENGTH	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	3/12/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Fairfield Health Products 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