FDA.reportPublic FDA data

AX Pharmaceutical Corp

Manufacturer
AX Pharmaceutical Corp
Effective date
2017-12-16
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:48:43

Label at a glance#

ProductAX Pharmaceutical Corp
Active ingredientBUTAFOSFAN
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-508-01AX Pharmaceutical Corp500 g in 1 JARPOWDER5001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-508AX PHARMACEUTICAL CORP (BUTAPHOSPHAN) POWDER [AX PHARMACEUTICAL CORP]11 package rows20171216_fd3a7c7f-2ca4-46db-9c8a-49d4e624684e.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 4 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62157-50862157-508-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 2 matching rows.

Name, UNII, Kind table
NameUNIIKind
BUTAFOSFAN3Q2LQ1149LACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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