NDC 64116-025-01 - AMPHOTEC

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
64116-025
Requested NDC
64116-025-01
Package NDCs from labels
64116-025-01
Manufacturer
InterMune, Inc.
Effective date
2006-02-27
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
AMPHOTEC® Amphotericin B Cholesteryl Sulfate Complex for InjectionInterMune, Inc.2006-02-27Human Prescription Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
64116-025-01AMPHOTEC10 mL in 1 VIAL, SINGLE-USEINJECTION, LIPID COMPLEX101

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
64116-025AMPHOTEC (AMPHOTERICIN B) INJECTION, LIPID COMPLEX [INTERMUNE, INC.]11 package rows20080313_9b8ea543-1de8-472f-9666-34f99ca2f183.zip

DailyMed Socrata Ingredients#

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 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4A32D598-0CAF-DBE7-12E3-4CD865EC9DF99b8ea543-1de8-472f-9666-34f99ca2f1832006-02-27Warnings, Adverse reactionsExact identifier
spl id: 4A32D598-0CAF-DBE7-12E3-4CD865EC9DF9
spl set id: 9b8ea543-1de8-472f-9666-34f99ca2f183

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.