FDA.reportPublic FDA data

NDC 71052-211-50 - Carprofen

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
71052-211
Requested NDC
71052-211-50
Package NDCs from labels
71052-211-01, 71052-211-25, 71052-211-10, 71052-211-50
Manufacturer
DARMERICA, LLC
Effective date
2026-01-09
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Carprofen - DARMERICA, LLCDARMERICA, LLC2026-01-09BULK INGREDIENT - ANIMAL DRUG

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71052-211-01Carprofen1 kg in 1 PACKAGEPOWDER14
71052-211-10Carprofen0.10 kg in 1 PACKAGEPOWDER0.104
71052-211-25Carprofen0.025 kg in 1 PACKAGEPOWDER0.0254
71052-211-50Carprofen0.50 kg in 1 PACKAGEPOWDER0.504

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71052-211CARPROFEN POWDER [DARMERICA, LLC]34 package rows20241222_2e2a3399-bffd-4429-8301-97d9470b0e05.zip

Reported adverse events (FAERS/openFDA)#

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