Allergy Relief

Product NDC
50090-4148
11-digit product format
500904148
Labeler code
50090
Product ID
50090-4148_a2ba02fd-1a98-4950-9c53-603744832310
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA075209
Marketing category
ANDA
Marketing start
2018-12-31
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-4148-0EA - Each50090-41485888f169-e3c5-4edf-9143-a273249a873c12022-01-06
50090-4148-3EA - Each50090-414873b9080b-d8c6-4512-8d38-eeace6f818b612022-01-06
50090-4148-4EA - Each50090-4148b16ffb31-ec67-4ae9-8e93-436e3a78d72812022-01-06
50090-4148-5EA - Each50090-4148d8432200-6d47-433f-a92e-5e3d4a72278612022-01-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-4148-05009041480010 TABLET in 1 BOTTLE (50090-4148-0) 10 tablet2019-02-190000-00-00NoNoCurrent
50090-4148-35009041480315 TABLET in 1 BOTTLE (50090-4148-3) 15 tablet2019-02-190000-00-00NoNoCurrent
50090-4148-45009041480430 TABLET in 1 BOTTLE, PLASTIC (50090-4148-4) 30 tablet2018-12-310000-00-00NoNoCurrent
50090-4148-55009041480590 TABLET in 1 BOTTLE, PLASTIC (50090-4148-5) 90 tablet2018-12-310000-00-00NoNoCurrent
50090-4148-6500904148067 TABLET in 1 BOTTLE (50090-4148-6) 7 tablet2019-02-190000-00-00NoNoCurrent