Allergy Relief

Product NDC
68998-309
11-digit product format
689980309
Labeler code
68998
Product ID
68998-309_8e89b50d-0514-417c-a0d1-b4b0b224f9df
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Marc Glassman, Inc.
Application
ANDA076471
Marketing category
ANDA
Marketing start
2014-12-16
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68998-309-85689980309852 BLISTER PACK in 1 CARTON (68998-309-85) > 15 TABLET in 1 BLISTER PACK2 blister pack2014-12-160000-00-00NoNoCurrent