Allergy Relief

Product NDC
53943-193
11-digit product format
539430193
Labeler code
53943
Product ID
53943-193_c6f315a9-9341-db6c-e053-2a95a90a1b2f
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
TABLET
Route
ORAL
Labeler
DISCOUNT DRUG MART
Application
ANDA210722
Marketing category
ANDA
Marketing start
2021-07-06
Substance
LORATADINE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
7AJO3BO7QNLORATADINE79794-75-5LORATADINE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
53943-193-18539430193182 BOTTLE, PLASTIC in 1 CARTON (53943-193-18) / 90 TABLET in 1 BOTTLE, PLASTIC2021-07-06NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
1193A-DDM-2021-0706DISCOUNT DRUG MART2021-07-12HUMAN OTC DRUG LABEL2