NDC 48102-054 - Phospholine Iodide

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
48102-054
Package NDCs from labels
48102-054-05
Manufacturer
Fera Pharmaceuticals, LLC
Effective date
2025-07-07
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
echothiophate iodide for ophthalmic solution - Fera Pharmaceuticals, LLCFera Pharmaceuticals, LLC2025-07-07HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
48102-054-05Phospholine Iodide6.25 mL in 1 BOTTLEPOWDER, FOR SOLUTION6.25 mL6.25 mg in 5mL5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
48102-054PHOSPHOLINE IODIDE (ECHOTHIOPHATE IODIDE FOR OPHTHALMIC SOLUTION) KIT [FERA PHARMACEUTICALS, LLC]4Unmatched20240913_8afc8951-db76-4f27-8752-7c0d6aa47244.zip