Harris Teeter Allergy Relief

Product NDC
69256-612
11-digit product format
692560612
Labeler code
69256
Product ID
69256-612_b5e50bd3-4505-42eb-96e9-fa851d1cfb04
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Harris Teeter, LLC
Application
ANDA076301
Marketing category
ANDA
Marketing start
2015-06-24
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69256-612-462025-01-30C16284748780-12cef2736-8f9e-d83d-e063-dadaa90ab31fHarris Teeter, LLC Allergy Relief Drug Facts
69256-612-652025-01-30C16284748780-12cef2736-8f9e-d83d-e063-dadaa90ab31fHarris Teeter, LLC Allergy Relief Drug Facts

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69256-612HARRIS TEETER ALLERGY RELIEF (LORATADINE) TABLET [HARRIS TEETER, LLC]3Legacy NDC20221201_a3bedebd-1fcc-44a1-a889-239c30600de5.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69256-612-466925606124610 BLISTER PACK in 1 CARTON (69256-612-46) > 1 TABLET in 1 BLISTER PACK10 blister pack2015-06-240000-00-00NoNoCurrent
69256-612-656925606126530 BOTTLE in 1 CARTON (69256-612-65) > 1 TABLET in 1 BOTTLE30 bottle2015-06-240000-00-00NoNoCurrent