42952-101 NDC - I-MAX EXCELLENCE ()

Drug Information

Product NDC: 42952-101

Proprietary Name: I-MAX EXCELLENCE

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: MAXLIFE USA, INC.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/15/2012

Package Information

No. Package Code Package Description Billing Unit
142952-101-1259 mL in 1 BOTTLE (42952-101-12)

NDC Record

Field Name Field Value Definition
PRODUCT NDC42952-101The 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 NAMEI-MAX EXCELLENCEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/15/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEMAXLIFE USA, INC.Name of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 8/16/2021