Allergy Relief-D 24 Hour

Product NDC
52544-239
11-digit product format
525440239
Labeler code
52544
Product ID
52544-239_c3b0d008-7d57-463f-b18e-e1ee694cdba6
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine and Pseudoephedrine Sulfate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Actavis Pharma, Inc.
Application
ANDA075706
Marketing category
ANDA
Marketing start
2018-06-14
Marketing end
2022-08-31
Substance
LORATADINE; PSEUDOEPHEDRINE SULFATE
Active strength
10 mg/1; mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
52544-239-12525440239123 BLISTER PACK in 1 CARTON (52544-239-12) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK3 blister pack2018-06-140000-00-00NoNoCurrent