51316-502 NDC - LORATADINE ()

Drug Information

Product NDC: 51316-502

Proprietary Name: LORATADINE

Non Proprietary Name:

Active Ingredient(s):


Administration Route(s):

Dosage Form(s):

Labeler Information

Labeler Name: CVS PHARMACY, INC
Product Type:
FDA Application Number:
Marketing Category:
Start Marketing Date:12/31/2021

Package Information

No. Package Code Package Description Billing Unit
151316-502-011 BLISTER PACK in 1 CARTON (51316-502-01) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
251316-502-022 BLISTER PACK in 1 CARTON (51316-502-02) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
351316-502-033 BLISTER PACK in 1 CARTON (51316-502-03) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
451316-502-044 BLISTER PACK in 1 CARTON (51316-502-04) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
551316-502-055 BLISTER PACK in 1 CARTON (51316-502-05) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK
651316-502-066 BLISTER PACK in 1 CARTON (51316-502-06) / 10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK

NDC Record

Field Name Field Value Definition
PRODUCT NDC51316-502The 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 NAMELORATADINEThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
START MARKETING DATE12/31/2021This is the date that the labeler indicates was the start of its marketing of the drug product.
LABELER NAMECVS PHARMACY, INCName 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