Allergy Relief

Product NDC
30142-555
11-digit product format
301420555
Labeler code
30142
Product ID
30142-555_a8b9c145-3b7a-4434-9a1b-cc3f0094db9c
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine HCl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Kroger Company
Application
ANDA076447
Marketing category
ANDA
Marketing start
2013-12-19
Marketing end
0000-00-00
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
60 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
30142-555-533014205555312 BLISTER PACK in 1 CARTON (30142-555-53) > 1 TABLET, FILM COATED in 1 BLISTER PACK12 blister pack2013-12-190000-00-00NoNoCurrent