73921-023 NDC - L-ORAL ALLERGEX HAY FEVER AND ALLERGY RELIEF SYRUP ()

Drug Information

Product NDC: 73921-023

Proprietary Name: L-Oral ALLERGEX Hay Fever and Allergy Relief Syrup

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: GLOBAL PHARMA HEALTHCARE PRIVATE LIMITED
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:4/1/2021

Package Information

No. Package Code Package Description Billing Unit
173921-023-041 BOTTLE, PLASTIC in 1 CARTON (73921-023-04) / 118 mL in 1 BOTTLE, PLASTIC

NDC Record

Field Name Field Value Definition
PRODUCT NDC73921-023The 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 NAMEL-Oral ALLERGEX Hay Fever and Allergy Relief SyrupThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE4/1/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEGLOBAL PHARMA HEALTHCARE PRIVATE LIMITEDName 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