50795-2001 NDC - U-MAX MULTI BB ()

Drug Information

Product NDC: 50795-2001

Proprietary Name: U-max Multi BB

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: VS Shinbi Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:6/4/2012

Package Information

No. Package Code Package Description Billing Unit
150795-2001-130 mL in 1 BOTTLE, WITH APPLICATOR (50795-2001-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50795-2001The 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 NAMEU-max Multi BBThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE6/4/2012This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEVS Shinbi Co., Ltd.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