Leader Allergy Relief D-24

Product NDC
37205-348
11-digit product format
372050348
Labeler code
37205
Product ID
37205-348_3c4eaae3-d16a-455b-98de-9fc32853bdb5
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine and Pseudoephedrine Sulfate
Dosage form
TABLET, FILM COATED, EXTENDED RELEASE
Route
ORAL
Labeler
Cardinal Health
Application
ANDA076557
Marketing category
ANDA
Marketing start
2004-11-17
Marketing end
0000-00-00
Substance
LORATADINE; PSEUDOEPHEDRINE SULFATE
Active strength
10 mg/1; mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
37205-348-52EA - Each37205-348a931f5a6-e211-4bac-9486-a40e0853503912012-07-24
37205-348-88EA - Each37205-3485f0e401c-3ba6-4cd2-ac8b-c5ae1722a75f12012-07-24