44929-002 NDC - CLEANOZ ()

Drug Information

Product NDC: 44929-002

Proprietary Name: Cleanoz

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Laboratoires Gifrer Barbezat
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	11/25/2008

No.	Package Code	Package Description
1	44929-002-02	20 AMPULE in 1 CARTON (44929-002-02) / 5 mL in 1 AMPULE (44929-002-01)
2	44929-002-03	3 AMPULE in 1 CARTON (44929-002-03) / 5 mL in 1 AMPULE (44929-002-01)
3	44929-002-04	5 AMPULE in 1 CARTON (44929-002-04) / 5 mL in 1 AMPULE (44929-002-01)
4	44929-002-05	40 AMPULE in 1 CARTON (44929-002-05) / 5 mL in 1 AMPULE (44929-002-01)
5	44929-002-06	10 AMPULE in 1 CARTON (44929-002-06) / 5 mL in 1 AMPULE (44929-002-01)
6	44929-002-07	30 AMPULE in 1 CARTON (44929-002-07) / 5 mL in 1 AMPULE (44929-002-01)

Field Name	Field Value	Definition
PRODUCT NDC	44929-002	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	Cleanoz	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	11/25/2008	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Laboratoires Gifrer Barbezat	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