Allergy Relief-D

Product NDC
41250-239
11-digit product format
412500239
Labeler code
41250
Product ID
41250-239_f4b96094-f1ed-4597-ba7a-17e7031d64d3
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine and Pseudoephedrine Sulfate
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
MEIJER, INC.
Application
ANDA075706
Marketing category
ANDA
Marketing start
2016-03-01
Marketing end
2024-04-26
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

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
41250-239-12EA - Each41250-239f9b4e9dc-a232-4573-a0ed-2cf8435c5a1912016-12-07
41250-239-79EA - Each41250-23938294f9e-e8ad-4845-a714-4b1bc6b46c6812016-12-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
41250-239-12412500239123 BLISTER PACK in 1 CARTON (41250-239-12) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK3 blister pack2016-04-010000-00-00NoNoCurrent
41250-239-79412500239792 BLISTER PACK in 1 CARTON (41250-239-79) > 5 TABLET, EXTENDED RELEASE in 1 BLISTER PACK2 blister pack2016-03-010000-00-00NoNoCurrent