49726-029 NDC - LICENEX ()

Drug Information

Product NDC: 49726-029

Proprietary Name: Licenex

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Hello Life, Inc.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/1/2013

Package Information

No. Package Code Package Description Billing Unit
149726-029-041 BOTTLE in 1 CARTON (49726-029-04) / 118 mL in 1 BOTTLE
249726-029-121 BOTTLE in 1 CARTON (49726-029-12) / 354 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC49726-029The 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 NAMELicenexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/1/2013This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEHello Life, 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