NDC 48201-015 - Angidol Raspberry

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
48201-015
Package NDCs from labels
48201-015-18
Manufacturer
GRANDALL DISTRIBUTING, LLC
Effective date
2024-01-23
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Angidol Raspberry - GRANDALL DISTRIBUTING, LLCGRANDALL DISTRIBUTING, LLC2024-01-23HUMAN OTC DRUG LABEL

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48201-015ANGIDOL RASPBERRY (BENZOCAINE, MENTHOL) LOZENGE [GRANDALL DISTRIBUTING, LLC]3Unmatched20240124_f7af356e-71ae-ca84-e053-6294a90a3b62.zip