FDA.reportPublic FDA data

smart sense allergy and congestion relief d

Product NDC
49738-118
11-digit product format
497380118
Labeler code
49738
Product ID
49738-118_eac3922f-c494-4da5-92cf-f2f5a196e968
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine, Pseudoephedrine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Kmart Corporation
Application
ANDA076050
Marketing category
ANDA
Marketing start
2015-07-29
Marketing end
0000-00-00
Substance
LORATADINE; PSEUDOEPHEDRINE SULFATE
Active strength
5 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
49738-118-522020-02-06C16284748780-19d75b9d0-a60f-f424-e053-dadaa90a57ce055ab06b-297e-41fa-ae82-d35667665721
49738-118-602020-02-06C16284748780-19d75b9d0-a60f-f424-e053-dadaa90a57ce055ab06b-297e-41fa-ae82-d35667665721
49738-118-522020-01-31C16284748780-19d75b9d0-a60f-f424-e053-dadaa90a57ce055ab06b-297e-41fa-ae82-d35667665721
49738-118-602020-01-31C16284748780-19d75b9d0-a60f-f424-e053-dadaa90a57ce055ab06b-297e-41fa-ae82-d35667665721