59321-011 NDC - GOLD EDITION ULTRA ZHENG GU SHUI ()

Drug Information

Product NDC: 59321-011

Proprietary Name: Gold Edition Ultra Zheng Gu Shui

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Guangxi Yulin Pharmaceutical Group Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/31/2022

Package Information

No. Package Code Package Description Billing Unit
159321-011-881 BOTTLE in 1 BOX (59321-011-88) / 88 mL in 1 BOTTLE

NDC Record

Field Name Field Value Definition
PRODUCT NDC59321-011The 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 NAMEGold Edition Ultra Zheng Gu ShuiThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/31/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGuangxi Yulin Pharmaceutical Group 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: 4/12/2024