Allergy relief

Product NDC
57896-687
11-digit product format
578960687
Labeler code
57896
Product ID
57896-687_b672eadc-d0d8-8382-e053-2a95a90a7572
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Geri-Care Pharmaceutical Corp
Application
ANDA075209
Marketing category
ANDA
Marketing start
2019-06-01
Marketing end
2022-01-01
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
57896-687-035789606870330 TABLET in 1 BOTTLE (57896-687-03) 30 tablet2019-06-012022-01-01NoNoCurrent
57896-687-095789606870990 TABLET in 1 BOTTLE (57896-687-09) 90 tablet2019-06-012022-01-01NoNoCurrent