Loratadine

Product NDC
0363-9955
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Walgreens Company
Application
ANDA212795
Marketing category
ANDA
Substance
LORATADINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
0363-9955-303 BLISTER PACK in 1 CARTON (0363-9955-30) / 10 TABLET in 1 BLISTER PACK2023-07-14NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Loratadine Orally Disintegrating Tablets USPWalgreens Company2023-02-27HUMAN OTC DRUG LABEL1