Allergy Relief

Product NDC
50090-5067
11-digit product format
500905067
Labeler code
50090
Product ID
50090-5067_3cf50eda-2af6-4e9c-ab40-1201d2377281
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
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
2021-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-5067-05009050670010 TABLET in 1 BOTTLE (50090-5067-0) 10 tablet2020-05-290000-00-00NoNoCurrent
50090-5067-15009050670120 TABLET in 1 BOTTLE (50090-5067-1) 20 tablet2020-05-290000-00-00NoNoCurrent
50090-5067-35009050670315 TABLET in 1 BOTTLE (50090-5067-3) 15 tablet2020-05-290000-00-00NoNoCurrent
50090-5067-45009050670430 TABLET in 1 BOTTLE (50090-5067-4) 30 tablet2020-05-290000-00-00NoNoCurrent
50090-5067-55009050670590 TABLET in 1 BOTTLE (50090-5067-5) 90 tablet2020-05-290000-00-00NoNoCurrent
50090-5067-6500905067067 TABLET in 1 BOTTLE (50090-5067-6) 7 tablet2020-05-290000-00-00NoNoCurrent