ALLERGY RELIEF

Product NDC
53943-192
11-digit product format
539430192
Labeler code
53943
Product ID
53943-192_d1cc33c6-c774-4f7c-e053-2a95a90ac116
Type
HUMAN OTC DRUG
Nonproprietary name
Fexofenadine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
DISCOUNT DRUG MART
Application
ANDA204507
Marketing category
ANDA
Marketing start
2020-01-03
Marketing end
2022-07-31
Substance
FEXOFENADINE HYDROCHLORIDE
Active strength
180 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 formatDescriptionMarketing startMarketing endSampleExclude flagStatus
53943-192-04539430192041 BOTTLE, PLASTIC in 1 CARTON (53943-192-04) > 30 TABLET in 1 BOTTLE, PLASTIC2020-01-030000-00-00NoNoCurrent
53943-192-06539430192061 BOTTLE, PLASTIC in 1 CARTON (53943-192-06) > 45 TABLET in 1 BOTTLE, PLASTIC2020-01-030000-00-00NoNoCurrent