7 Select Allergy Relief

Product NDC
10202-612
11-digit product format
102020612
Labeler code
10202
Product ID
10202-612_3900f606-400c-44ba-8d52-b6c6ee1e12d3
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
7-Eleven
Application
ANDA076301
Marketing category
ANDA
Marketing start
2014-05-14
Marketing end
2020-10-31
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record