Childrens Loratadine

Product NDC
41520-085
11-digit product format
415200085
Labeler code
41520
Product ID
41520-085_c09b23f3-4ca7-44fd-aec5-7cf6e5f4253b
Type
HUMAN OTC DRUG
Nonproprietary name
Loratadine
Dosage form
SOLUTION
Route
ORAL
Labeler
American Sales Company
Application
ANDA076805
Marketing category
ANDA
Marketing start
2004-08-20
Marketing end
0000-00-00
Substance
LORATADINE
Active strength
5 mg/5mL
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
41520-085-082020-01-31C16284748780-19d75b9d0-3b53-f424-e053-dadaa90a57ceChildren's Loratadine

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
41520-085-08Childrens Loratadine1 in 1 CARTONSOLUTION11
41520-085-08Childrens Loratadine118 mL in 1 BOTTLESOLUTION1181

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
41520-085CHILDRENS LORATADINE (LORATADINE) SOLUTION [AMERICAN SALES COMPANY]1Legacy NDC, 2 package rows20121121_bbcba43e-5657-4272-b196-cd81033ab192.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
692783loratadine 5 MG in 5 mL Oral SolutionPSNbbcba43e-5657-4272-b196-cd81033ab1921
692783loratadine 1 MG/ML Oral SolutionSCDbbcba43e-5657-4272-b196-cd81033ab1921
692783loratadine 5 MG per 5 ML Oral SolutionSYbbcba43e-5657-4272-b196-cd81033ab1921

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
41520-085-08415200085081 in 1 CARTONHistorical