36800-528 NDC - LORATADINE ODT ()

Drug Information

Product NDC: 36800-528

Proprietary Name: Loratadine ODT

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: Topco Associates LLC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:8/31/2007

Package Information

No. Package Code Package Description Billing Unit
136800-528-6910 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (36800-528-69)

NDC Record

Field Name Field Value Definition
PRODUCT NDC36800-528The 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 NAMELoratadine ODTThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE8/31/2007This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMETopco Associates LLCName of Company corresponding to the labeler code segment of the Product NDC.

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

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