77598-126 NDC - ALLORA ()

Drug Information

Product NDC: 77598-126

Proprietary Name: Allora

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Guangzhou Ouzhuang Biological Technology Co Ltd
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:5/15/2020

Package Information

No. Package Code Package Description Billing Unit
177598-126-0130 mL in 1 BOTTLE (77598-126-01)
277598-126-0260 mL in 1 BOTTLE (77598-126-02)
377598-126-03100 mL in 1 BOTTLE (77598-126-03)
477598-126-04300 mL in 1 BOTTLE (77598-126-04)
577598-126-05500 mL in 1 BOTTLE (77598-126-05)
677598-126-061000 mL in 1 BOTTLE (77598-126-06)
777598-126-073800 mL in 1 BOTTLE (77598-126-07)
877598-126-085000 mL in 1 BOTTLE (77598-126-08)

NDC Record

Field Name Field Value Definition
PRODUCT NDC77598-126The 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 NAMEAlloraThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE5/15/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGuangzhou Ouzhuang Biological Technology Co LtdName 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