FDA.reportPublic FDA data

X

Manufacturer
AX Pharmaceutical Corp
Effective date
2015-12-03
Label type
BULK INGREDIENT
Version
2
Source
full-release
Hydrated at
2026-06-01 02:48:09

Label at a glance#

ProductX
Active ingredientPHENYLBUTAZONE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

copy of labelcopy of label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
62157-119-01X25000 g in 1 DRUMPOWDER250002

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
62157-119X (PHENYLBUTAZONE) POWDER [AX PHARMACEUTICAL CORP]21 package rows20151204_cd395cf1-5dd2-4b42-9cb7-2bbbf703c8ac.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
PHENYLBUTAZONEACTIVE INGREDIENTGN5P7K3T8S1
PHENYLBUTAZONEACTIVE MOIETYGN5P7K3T8S1
WATERINACTIVE INGREDIENT059QF0KO0R1

Products#

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

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
62157-11962157-119-01

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
PHENYLBUTAZONEGN5P7K3T8SACTIB
WATER059QF0KO0RIACT

Source Document#

Source XML · Source PDF

Reported adverse events (FAERS/openFDA)#

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