All Day Allergy Relief

Product NDC
83324-146
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
QUALITY CHOICE (Chain Drug Marketing Association)
Application
ANDA075209
Marketing category
ANDA
Substance
LORATADINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
83324-146-301 BOTTLE, PLASTIC in 1 BOX (83324-146-30) / 30 TABLET in 1 BOTTLE, PLASTIC2024-07-31NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsQUALITY CHOICE (Chain Drug Marketing Association)2024-06-17HUMAN OTC DRUG LABEL2