Allergy Relief

Product NDC
63868-414
11-digit product format
638680414
Labeler code
63868
Product ID
63868-414_67979878-1de4-4f50-b2cb-0bfed40faa89
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
QUALITY CHOICE (Chain Drug Marketing Association)
Application
ANDA075209
Marketing category
ANDA
Marketing start
2021-04-15
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
63868-414-01EA - Each63868-4148325f9b1-ac69-4ccf-86a4-c7081364d9e712022-10-06

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
63868-414ALLERGY RELIEF (LORATADINE) TABLET [QUALITY CHOICE (CHAIN DRUG MARKETING ASSOCIATION)]3Legacy NDC20241102_dff47a40-0c3e-4fa3-a347-e60ce0c3b8b7.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
63868-414-01638680414011 BOTTLE, PLASTIC in 1 BOX (63868-414-01) > 100 TABLET in 1 BOTTLE, PLASTIC2021-04-150000-00-00NoNoCurrent