75622-622 NDC - DEYO ()

Drug Information

Product NDC: 75622-622

Proprietary Name: DEYO

Non Proprietary Name:

Active Ingredient(s):

Administration Route(s):

Dosage Form(s):

Labeler Name:	Henan Yeesain Health Technology Co., Ltd.
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:	5/1/2020

No.	Package Code	Package Description
1	75622-622-10	10 NOT APPLICABLE in 1 POUCH (75622-622-10) / 6.2 mL in 1 NOT APPLICABLE
2	75622-622-20	40 NOT APPLICABLE in 1 POUCH (75622-622-20) / 6.2 mL in 1 NOT APPLICABLE
3	75622-622-30	50 NOT APPLICABLE in 1 CANISTER (75622-622-30) / 50 mL in 1 NOT APPLICABLE
4	75622-622-40	80 NOT APPLICABLE in 1 CANISTER (75622-622-40) / 80 mL in 1 NOT APPLICABLE
5	75622-622-50	100 NOT APPLICABLE in 1 CANISTER (75622-622-50) / 100 mL in 1 NOT APPLICABLE

Field Name	Field Value	Definition
PRODUCT NDC	75622-622	The 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 NAME	DEYO	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 DATE	5/1/2020	This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAME	Henan Yeesain Health Technology 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