49795-227 NDC - PRO-FLEX ()

Drug Information

Product NDC: 49795-227

Proprietary Name: Pro-Flex

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Nutri-Dyn Products Ltd. dba Professional Health Products
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	2/1/2004

No.	Package Code	Package Description
1	49795-227-01	120 g in 1 JAR (49795-227-01)
2	49795-227-02	500 g in 1 BOTTLE, PLASTIC (49795-227-02)
3	49795-227-03	5 g in 1 JAR (49795-227-03)

Field Name	Field Value	Definition
PRODUCT NDC	49795-227	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	Pro-Flex	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	2/1/2004	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Nutri-Dyn Products Ltd. dba Professional Health Products	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