FDA.reportPublic FDA data

Decoquinate

Manufacturer
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Effective date
2014-04-25
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:47:56

Label at a glance#

ProductDecoquinate
Active ingredientDecoquinate
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
58597-8214-1Decoquinate1 g in 1 BOTTLEPOWDER11
58597-8214-2Decoquinate5 g in 1 BOTTLEPOWDER51
58597-8214-4Decoquinate25 g in 1 BOTTLEPOWDER251
58597-8214-5Decoquinate50 g in 1 BOTTLEPOWDER501

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58597-8214DECOQUINATE POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC]14 package rows20140428_de2fb483-0876-4d49-bc24-e0f72c70aa63.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
DecoquinateACTIVE INGREDIENT534I52PVWH1
DecoquinateACTIVE MOIETY534I52PVWH1

Products#

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

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
58597-821458597-8214-1, 58597-8214-2, 58597-8214-4, 58597-8214-5

Ingredients#

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

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

Name, UNII, Kind table
NameUNIIKind
Decoquinate534I52PVWHACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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