NDC 48951-8408 - Strophanthus 4X

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
48951-8408
Package NDCs from labels
48951-8408-3
Manufacturer
Uriel Pharmacy Inc.
Effective date
2024-01-29
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Strophanthus 4XUriel Pharmacy Inc.2024-01-29HUMAN OTC DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48951-8408-3Strophanthus 4X60 mL in 1 BOTTLE, DROPPERLIQUID601

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48951-8408STROPHANTHUS 4X LIQUID [URIEL PHARMACY INC.]11 package rows20240130_101bbd35-afed-e680-e063-6394a90afcfa.zip