61941-0132 NDC - ORGANIX COMPLETE ()

Drug Information

Product NDC: 61941-0132

Proprietary Name: Organix Complete

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: ProPhase Labs, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:11/1/2010

Package Information

No. Package Code Package Description Billing Unit
161941-0132-248 PACKAGE in 1 CASE (61941-0132-2) / 21 LOZENGE in 1 PACKAGE (61941-0132-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC61941-0132The 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 NAMEOrganix CompleteThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE11/1/2010This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEProPhase Labs, 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