Allergy Relief

Product NDC
37012-612
11-digit product format
370120612
Labeler code
37012
Product ID
37012-612_105d6e7a-e8d5-43d3-bdd7-561d71217bde
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA076301
Marketing category
ANDA
Marketing start
2013-09-12
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37012-612-03370120612031 BOTTLE in 1 CARTON (37012-612-03) > 70 TABLET in 1 BOTTLE1 bottle2016-08-030000-00-00NoNoCurrent
37012-612-463701206124610 BLISTER PACK in 1 CARTON (37012-612-46) > 1 TABLET in 1 BLISTER PACK10 blister pack2013-09-120000-00-00NoNoCurrent
37012-612-65370120612651 BOTTLE in 1 CARTON (37012-612-65) > 30 TABLET in 1 BOTTLE1 bottle2013-09-190000-00-00NoNoCurrent
37012-612-72370120612721 BOTTLE in 1 CARTON (37012-612-72) > 60 TABLET in 1 BOTTLE1 bottle2013-10-170000-00-00NoNoCurrent
37012-612-95370120612951 BOTTLE in 1 CARTON (37012-612-95) > 45 TABLET in 1 BOTTLE1 bottle2016-12-010000-00-00NoNoCurrent