Allergy Relief

Product NDC
83324-103
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
CHAIN DRUG MARKETING ASSOCIATION, INC.
Application
ANDA206214
Marketing category
ANDA
Substance
LORATADINE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
83324-103-101 BLISTER PACK in 1 CARTON (83324-103-10) / 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK2024-08-12NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1195A-QCH-2024-0812CHAIN DRUG MARKETING ASSOCIATION, INC.2024-08-12HUMAN OTC DRUG LABEL2