Home NDC 51672-2131-01 NDC 51672-2131-01 - Childrens Loratadine Sugar Free This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
Product NDC 51672-2131
Requested NDC 51672-2131-01
Package NDCs from labels 51672-2131-4, 51672-2131-8, 51672-2131-1, 51672-2131-01
Manufacturer Sun Pharmaceutical Industries, Inc. | Sun Pharma Canada Inc. | Taro Pharmaceutical Industries, Ltd.
Effective date 2026-08-30
Current FDA listing Not matched in FDA.report NDC product tables DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 51672-2131-1 Childrens LoratadineSugar Free 1 in 1 CARTON SOLUTION 1 4 51672-2131-1 Childrens LoratadineSugar Free 240 mL in 1 BOTTLE SOLUTION 240 4 51672-2131-4 Childrens LoratadineSugar Free 60 mL in 1 BOTTLE SOLUTION 60 4 51672-2131-4 Childrens LoratadineSugar Free 1 in 1 CARTON SOLUTION 1 4 51672-2131-8 Childrens LoratadineSugar Free 120 mL in 1 BOTTLE SOLUTION 120 4 51672-2131-8 Childrens LoratadineSugar Free 1 in 1 CARTON SOLUTION 1 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 51672-2131 CHILDRENS LORATADINE SUGAR FREE (LORATADINE) SOLUTION [TARO PHARMACEUTICALS U.S.A., INC.] 3 Current NDC, Legacy NDC, 6 package rows 20230805_58eaab62-ac36-4080-8ded-9b472dddc617.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 11 of 61 · 1,213 matching rows.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.