7 Select Allergy Relief

Product NDC
10202-571
11-digit product format
102020571
Labeler code
10202
Product ID
10202-571_24688cdc-86d0-43b0-b78d-ae6028f81eb4
Type
HUMAN OTC DRUG
Nonproprietary name
fexofenadine hcl
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
7-Eleven
Application
ANDA076447
Marketing category
ANDA
Marketing start
2014-04-17
Marketing end
2020-07-31
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