Allergy Relief

Product NDC
69230-317
11-digit product format
692300317
Labeler code
69230
Product ID
69230-317_9f76f1cf-82cb-4986-a72e-29a6338c12eb
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Camber Consumer Care
Application
ANDA075209
Marketing category
ANDA
Marketing start
2019-12-27
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
69230-317-01EA - Each69230-3170cd55077-187c-480b-9e02-f69396dd0a2712020-06-05
69230-317-03EA - Each69230-3177a46899f-8a8f-44cb-915b-673c9fb7e35312020-06-05

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69230-317ALLERGY RELIEF NON DROWSY (LORATADINE) TABLET [CAMBER CONSUMER CARE]5Legacy NDC20241206_e2e5fe3b-6bf1-4f93-9713-a03159b1699e.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
69230-317-01692300317011 BOTTLE, PLASTIC in 1 BOX (69230-317-01) > 100 TABLET in 1 BOTTLE, PLASTIC2019-12-270000-00-00NoNoCurrent
69230-317-0369230031703300 TABLET in 1 BOTTLE, PLASTIC (69230-317-03) 300 tablet2019-12-270000-00-00NoNoCurrent
69230-317-30692300317301 BOTTLE, PLASTIC in 1 BOX (69230-317-30) > 30 TABLET in 1 BOTTLE, PLASTIC2019-12-270000-00-00NoNoCurrent