Loratadine

Product NDC
16714-482
11-digit product format
167140482
Labeler code
16714
Product ID
16714-482_f6946e6a-bff4-4115-9f0f-d4734d769151
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Northstar RxLLC
Application
ANDA075209
Marketing category
ANDA
Marketing start
2016-02-01
Marketing end
2020-12-31
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16714-482-01EA - Each16714-4821ca1fb9d-283e-477e-9b0e-d5f29f0419ee12016-03-04
16714-482-02EA - Each16714-48257fd7507-d577-42a2-a12a-17a032f9dac812016-03-04
16714-482-03EA - Each16714-482cb32ac90-06cc-4eae-823a-528a5728934212016-03-04

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
311372loratadine 10 MG 24HR Oral TabletPSNeb7196aa-898b-48d3-a6c7-8b52ff740b303
311372loratadine 10 MG Oral TabletSCDeb7196aa-898b-48d3-a6c7-8b52ff740b303
311372loratadine 10 MG 24 HR Oral TabletSYeb7196aa-898b-48d3-a6c7-8b52ff740b303
311372loratadine 10 MG 24HR Oral TabletPSN0c5a71f2-ffec-47aa-8283-6297a02c75811
311372loratadine 10 MG Oral TabletSCD0c5a71f2-ffec-47aa-8283-6297a02c75811
311372loratadine 10 MG 24 HR Oral TabletSY0c5a71f2-ffec-47aa-8283-6297a02c75811