NDC 69043-031-60 - 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: 69043-031
Requested NDC: 69043-031-60
Package NDCs from labels: 69043-031-60, 69043-031-18
Manufacturer: Cronus Pharma LLC
Effective date: 2025-08-26
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Carprofen - Cronus Pharma LLC	Cronus Pharma LLC	2025-08-26	Prescription Animal Drug Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
69043-031-18	Carprofen	180 in 1 BOTTLE	TABLET, CHEWABLE	180		5
69043-031-60	Carprofen	60 in 1 BOTTLE	TABLET, CHEWABLE	60		5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
69043-031	CARPROFEN TABLET, CHEWABLE [CRONUS PHARMA LLC]	4	2 package rows	20240725_3c088145-0f3e-4fb6-9b46-d53344de1b82.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Amoxicillin and Clavulanate Potassium	AMOXICILLIN AND CLAVULANATE POTASSIUM	Aurobindo Pharma Limited	3ae0c95f-7ffa-4317-9fea-4d07b86bee72	2026-08-13	Warnings, Adverse reactions	Exact identifier application number: ANDA209371

Reported adverse events (FAERS/openFDA)#

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