Allergy relief

Product NDC
57896-788
11-digit product format
578960788
Labeler code
57896
Product ID
57896-788_9aa07ca9-ee19-89c7-e053-2a95a90ae9b5
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Geri-Care Pharmaceutical Corp
Application
ANDA076471
Marketing category
ANDA
Marketing start
2008-01-01
Marketing end
2021-06-01
Substance
LORATADINE
Active strength
10 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
57896-788-03EA - Each57896-7883150a13c-0a0a-4c17-946a-67c73e3904f412017-04-05
57896-788-09EA - Each57896-7882ce245d4-f389-4b9c-a13f-ad630186988312018-02-20

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57896-788-035789607880330 TABLET in 1 BOTTLE (57896-788-03) 30 tablet2008-01-012021-06-01NoNoCurrent
57896-788-095789607880990 TABLET in 1 BOTTLE (57896-788-09) 90 tablet2008-01-012021-06-01NoNoCurrent