NDC 49994-316 - 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: 49994-316
Package NDCs from labels: 49994-316-81
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
Label	Manufacturer	Effective date	Type
TruProfen (Carprofen) Flavored Tablets	TruRx, LLC \| COSMA Spa \| PROCOS SpA \| Alivira Animal Health Limited \| AJENAT PHARMACEUTICALS LLC	2025-06-11	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
49994-316-81	TRUPROFEN FLAVORED TAB	180 in 1 BOTTLE, PLASTIC	TABLET, CHEWABLE	180		7

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
49994-316	TRUPROFEN FLAVORED TAB (CARPROFEN) TABLET, CHEWABLE [TRURX, LLC]	6	1 package rows	20241204_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 · 2 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
YVTYVT MICRODERMABRASION FACIAL SCRUB	YVTYVT MICRODERMABRASION FACIAL SCRUB	Beijing JUNGE Technology Co., Ltd.	2f30fc45-42e2-c766-e063-6394a90a8d68	2025-02-28	Warnings	Exact identifier unii: OP1R32D61U
Anubis Barcelona Spa Line	ORYZA SATIVA (RICE) STARCH, PERLITE, PALMITIC ACID	ANUBIS COSMETICS SL	eb01a962-ab38-18ec-e053-2995a90acdeb	2023-09-01	Warnings	Exact identifier unii: 4ELV7Z65AP

Reported adverse events (FAERS/openFDA)#

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