All Day Allergy Relief

Product NDC
55910-718
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application
ANDA075209
Marketing category
ANDA
Substance
LORATADINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
55910-718-301 BOTTLE, PLASTIC in 1 BOX (55910-718-30) / 30 TABLET in 1 BOTTLE, PLASTIC2023-10-25NoHistorical
55910-718-601 BOTTLE, PLASTIC in 1 BOX (55910-718-60) / 60 TABLET in 1 BOTTLE, PLASTIC2023-10-25NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsDolgencorp, Inc. (DOLLAR GENERAL & REXALL)2023-10-26HUMAN OTC DRUG LABEL3