Allergy Relief d 12

Product NDC
59779-013
11-digit product format
597790013
Labeler code
59779
Product ID
59779-013_1318fb77-52df-4814-b703-4655ec0c7efc
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine, Pseudoephedrine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
CVS Pharmacy
Application
ANDA076050
Marketing category
ANDA
Marketing start
2012-01-25
Marketing end
0000-00-00
Substance
LORATADINE; PSEUDOEPHEDRINE SULFATE
Active strength
5 mg/1; mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59779-013-39EA - Each59779-013e4e64975-5555-4104-9ab1-7c1ebae7e11112017-04-05
59779-013-52EA - Each59779-0132e04fc05-4473-4635-ad59-2eb995d75f4212017-04-05
59779-013-60EA - Each59779-01326bf5d63-23cb-44cb-8960-9a359023239412016-09-02