FDA.reportPublic FDA data

AX Pharmaceutical Corp

Manufacturer
AX Pharmaceutical Corp
Effective date
2017-12-05
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:48:41

Label at a glance#

ProductAX Pharmaceutical Corp
Active ingredientMETAMIZOLE SODIUM
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
62157-500-01AX Pharmaceutical Corp1 kg in 1 JARPOWDER11

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-500AX PHARMACEUTICAL CORP (METAMIZOLE SODIUM) POWDER [AX PHARMACEUTICAL CORP]11 package rows20171206_cdcb4a7d-c019-4f40-af37-2aa73ee1cd99.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
62157-50062157-500-01

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
METAMIZOLE SODIUMVSU62Z74ONACTIM
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

Reported adverse events (FAERS/openFDA)#

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