FDA.reportPublic FDA data

Carprofen

Manufacturer
Norbrook Laboratories Limited
Effective date
2017-05-15
Label type
BULK INGREDIENT - ANIMAL DRUG
Version
1
Source
full-release
Hydrated at
2026-06-01 02:49:33

Label at a glance#

ProductCarprofen
Active ingredientCarprofen
Label structure1 sections

Label contents#

Full prescribing information#

Principal Display Panel - Drum Label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CARPROFEN USP

Danger

CAS No. 53716-49-7

EC No. 258-712-4

Caution: For manufacturing, processing, or repacking.

Caution: Federal (U.S.A.) law restricts this drug to
use by or on the order of a licensed veterinarian.

Store below 25°C, protect from light.

For Veterinary Use Only.

NET WEIGHT: RESOURCE CODE:

BATCH NUMBER: DATE OF MANUFACTURE:

DRUM NUMBER: DATE OF EXPIRY:

Norbrook® Laboratories Limited

Newry, Co Down, BT35 6QQ

Northern Ireland

Tel: +44 (0)28 3026 4435

Fax: +44 (0)28 3026 1721

Email: enquiries@norbrook.co.uk

www.norbrook.com

Norbrook®

Principal Display Panel - Drum Label
Principal Display Panel - Drum Label

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
55529-620-32Carprofen10 kg in 1 DRUMPOWDER101
55529-620-33Carprofen25 kg in 1 DRUMPOWDER251

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
55529-620CARPROFEN POWDER [NORBROOK LABORATORIES LIMITED]12 package rows20200401_85fd0033-bfc2-4c44-942b-3d0c75b69fc6.zip

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
55529-62055529-620-32, 55529-620-33

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.