FDA.reportPublic FDA data

CISAPRIDE

Manufacturer
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Effective date
2014-05-02
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:47:57

Label at a glance#

ProductCISAPRIDE
Active ingredientCISAPRIDE
Label structure1 sections

Label contents#

Full prescribing information#

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a4e2baf7-73e6-4103-93f8-b19723717eafProduct name120201013

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
58597-8558-2CISAPRIDE5 g in 1 BOTTLEPOWDER51
58597-8558-4CISAPRIDE25 g in 1 BOTTLEPOWDER251
58597-8558-6CISAPRIDE100 g in 1 BOTTLEPOWDER1001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58597-8558CISAPRIDE POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC]13 package rows20140503_2c35b6e6-370e-4f1b-ba9c-3e07649d2973.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CISAPRIDEACTIVE INGREDIENTUVL329170W1
CISAPRIDEACTIVE MOIETYUVL329170W1

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
58597-855858597-8558-2, 58597-8558-4, 58597-8558-6

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
CISAPRIDEUVL329170WACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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