FDA.reportPublic FDA data

Carprofen

Manufacturer
AMERICAN PHARMACEUTICAL INGREDIENTS LLC
Effective date
2014-04-25
Label type
BULK INGREDIENT
Version
1
Source
full-release
Hydrated at
2026-06-01 02:47:55

Label at a glance#

ProductCarprofen
Active ingredientCarprofen
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
58597-8168-6Carprofen100 g in 1 BOTTLEPOWDER1001
58597-8168-7Carprofen500 g in 1 BOTTLEPOWDER5001
58597-8168-8Carprofen1000 g in 1 BOTTLEPOWDER10001
58597-8168-9Carprofen5000 g in 1 BOTTLEPOWDER50001

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
58597-8168CARPROFEN POWDER [AMERICAN PHARMACEUTICAL INGREDIENTS LLC]14 package rows20140426_cbbc4480-34ac-4d00-a7a3-61ed54cbbe1d.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
CarprofenACTIVE INGREDIENTFFL0D546HO1
CarprofenACTIVE MOIETYFFL0D546HO1

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
58597-816858597-8168-6, 58597-8168-7, 58597-8168-8, 58597-8168-9

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
CarprofenFFL0D546HOACTIB

Source Document#

Source XML

Reported adverse events (FAERS/openFDA)#

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