50090-5341 NDC - LEVOCETIRIZINE DIHYDROCHLORIDE ()

Drug Information

Product NDC: 50090-5341

Proprietary Name: Levocetirizine Dihydrochloride

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: A-S Medication Solutions
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:10/28/2020

Package Information

No. Package Code Package Description Billing Unit
150090-5341-030 TABLET, FILM COATED in 1 BOTTLE (50090-5341-0)
250090-5341-190 TABLET, FILM COATED in 1 BOTTLE (50090-5341-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50090-5341The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
PROPRIETARY NAMELevocetirizine DihydrochlorideThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE10/28/2020This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMEA-S Medication SolutionsProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

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This page was last updated on: 2/1/2023