NDC 49994-318-81 - TRUPROFEN FLAVORED TAB

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
49994-318
Requested NDC
49994-318-81
Package NDCs from labels
49994-318-81
Manufacturer
TruRx, LLC | COSMA Spa | PROCOS SpA | Alivira Animal Health Limited | AJENAT PHARMACEUTICALS LLC
Effective date
2025-06-11
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
TruProfen (Carprofen) Flavored TabletsTruRx, LLC | COSMA Spa | PROCOS SpA | Alivira Animal Health Limited | AJENAT PHARMACEUTICALS LLC2025-06-11PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
49994-318-81TRUPROFEN FLAVORED TAB180 in 1 BOTTLE, PLASTICTABLET, CHEWABLE1807

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
49994-318TRUPROFEN FLAVORED TAB (CARPROFEN) TABLET, CHEWABLE [TRURX, LLC]61 package rows20241204_a4870fcd-e106-4a09-bcbd-8b0a61af267e.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 ยท 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
YVTYVT MICRODERMABRASION FACIAL SCRUBYVTYVT MICRODERMABRASION FACIAL SCRUBBeijing JUNGE Technology Co., Ltd.2f30fc45-42e2-c766-e063-6394a90a8d682025-02-28WarningsExact identifier
unii: OP1R32D61U
Anubis Barcelona Spa LineORYZA SATIVA (RICE) STARCH, PERLITE, PALMITIC ACIDANUBIS COSMETICS SLeb01a962-ab38-18ec-e053-2995a90acdeb2023-09-01WarningsExact identifier
unii: 4ELV7Z65AP

Reported adverse events (FAERS/openFDA)#

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