73750-104 NDC - VARDENAFIL HYDROCHLORIDE ()

Drug Information

Product NDC: 73750-104

Proprietary Name: Vardenafil Hydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: QYK BRANDS LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:3/1/2022

Package Information

No. Package Code Package Description Billing Unit
173750-104-10100 TABLET in 1 BOTTLE (73750-104-10)
273750-104-1110 BLISTER PACK in 1 CARTON (73750-104-11) / 10 TABLET in 1 BLISTER PACK
373750-104-3030 TABLET in 1 BOTTLE (73750-104-30)

NDC Record

Field Name Field Value Definition
PRODUCT NDC73750-104The 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 NAMEVardenafil HydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE3/1/2022This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEQYK BRANDS LLCName 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