47649-9001 NDC - DR. WHITISS (8.3%) ()

Drug Information

Product NDC: 47649-9001

Proprietary Name: Dr. Whitiss (8.3%)

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Nibec Co., Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:7/11/2014

Package Information

No. Package Code Package Description Billing Unit
147649-9001-15 g in 1 PACKAGE (47649-9001-1)
247649-9001-34 CYLINDER in 1 PACKAGE (47649-9001-3) / 2 g in 1 CYLINDER (47649-9001-2)

NDC Record

Field Name Field Value Definition
PRODUCT NDC47649-9001The 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 NAMEDr. Whitiss (8.3%)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 DATE7/11/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMENibec Co., LtdName of Company corresponding to the labeler code segment of the Product NDC.

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This page was last updated on: 4/12/2024