careone allergy relief

Product NDC
41520-510
11-digit product format
415200510
Labeler code
41520
Product ID
41520-510_bb4f118d-ddd4-407a-9a07-0660c6150ca6
Type
HUMAN OTC DRUG
Nonproprietary name
loratadine
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
American Sales Company
Application
ANDA076011
Marketing category
ANDA
Marketing start
2021-11-08
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 formatDescriptionUnitsMarketing startSampleExclude flagStatus
41520-510-654152005106530 BLISTER PACK in 1 CARTON (41520-510-65) / 1 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK30 blister pack2021-11-08NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
American Sales Company Allergy Relief Drug FactsAmerican Sales Company2021-11-15HUMAN OTC DRUG LABEL2