Allergy Relief D

Product NDC
37012-013
11-digit product format
370120013
Labeler code
37012
Product ID
37012-013_a290d25a-d6fb-4e95-848a-c42b2b4992fd
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine, Pseudoephedrine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA076050
Marketing category
ANDA
Marketing start
2013-10-02
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
37012-013-602021-05-25C16284748780-19d75b9d0-2dc7-f424-e053-dadaa90a57ce145444df-b2ed-4cc8-b35f-420160a1d9be
37012-013-602020-01-31C16284748780-19d75b9d0-2dc7-f424-e053-dadaa90a57ce145444df-b2ed-4cc8-b35f-420160a1d9be