Fatal-Plus Powder

Manufacturer
Vortech Pharmaceuticals, Ltd. | Vortech Pharmaceuticals, Ltd | Siegfried USA, LLC
Effective date
2016-12-21
Label type
PRESCRIPTION ANIMAL DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 02:40:01

Label at a glance#

ProductFatal-Plus Powder
Active ingredientPentobarbital Sodium
Label structure2 sections

Label contents#

Full prescribing information#

Description

DESCRIPTION SECTION

Fatal-Plus Powder

Pentobarbital Sodium - 98 grams

FOR VETERINARY USE ONLY

For Euthanasia of Animals

DIRECTIONS FOR MIXING:

Slowly add water (150 mL to 200 mL).

Replace cap and shake well until powder is dissolved.

Add more water to the 250 mL mark only.

Do not exceed the fill line (250 mL).

DOSAGE AND ADMINISTRATION:

Intravenous injection is the preferred route.  However, intraperitoneal or intracardiac injections may be made where the intravenous injection is impractical, as in the very small dog and cat, or in the comatose animal with depressed vascular function.  Inject rapidly 1 mL for every 10 lbs. body weight  Minimum 1 mL.

WARNING:  Must not be used for therapeutic purposes.  Do not use in animals intended for food.
ENVIRONMENTAL HAZARD:

This product is toxic to wildlife.  Birds and mammals feeding on treated animals may be killed.  Birds and mammals feeding on treated animals may be killed.  Euthanized animals must be properly disposed of by deep burial, incineration, or other method in compliance with state and local laws, to prevent consumption of carcass material by scavenging wildlife.

CAUTION:  Federal law restricts this drug to use by or on the order of a licensed veterinarian.

POISON:  KEEP OUT OF THE REACH OF CHILDREN

Principle Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Fatal-Plus Powder - NDC: 0298-9372-68

Pentobarbital Sodium - 98 grams

FOR VETERINARY USE ONLY

For Euthanasia of Animals

DIRECTIONS FOR MIXING:

Slowly add water (150 mL to 200 mL).

Replace cap and shake well until powder is dissolved.

Add more water to the 250 mL mark only.

Do not exceed the fill line (250 mL).

DOSAGE AND ADMINISTRATION:

Intravenous injection is the preferred route.  However, intraperitoneal or intracardiac injections may be made where the intravenous injection is impractical, as in the very small dog and cat, or in the comatose animal with depressed vascular function.  Inject rapidly 1 mL for every 10 lbs. body weight  Minimum 1 mL.

WARNING:  Must not be used for therapeutic purposes.  Do not use in animals intended for food.

ENVIRONMENTAL HAZARD:

This product is toxic to wildlife.  Birds and mammals feeding on treated animals may be killed.  Birds and mammals feeding on treated animals may be killed.  Euthanized animals must be properly disposed of by deep burial, incineration, or other method in compliance with state and local laws, to prevent consumption of carcass material by scavenging wildlife.

CAUTION:  Federal law restricts this drug to use by or on the order of a licensed veterinarian.

POISON: 

KEEP OUT OF THE REACH OF CHILDREN
powderpowder

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1602561pentobarbital sodium 392 MG/ML Injectable Solution [Fatal-Plus]SBD2
1099882pentobarbital sodium 392 MG/ML Injectable SolutionSCD2
1602561Fatal-Plus 392 MG/ML Injectable SolutionSY2

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a608f88c-baa8-0098-ce26-66cf9faa6b64Product name320180110

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0298-9372-68Fatal-Plus Powder250 mL in 1 VIAL, MULTI-DOSEINJECTION, SOLUTION2502

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0298-9372FATAL-PLUS POWDER (PENTOBARBITAL SODIUM) INJECTION, SOLUTION [VORTECH PHARMACEUTICALS, LTD.]21 package rows20161221_4fd5c64f-8560-4459-b0a5-92db95de4e74.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIISPL versionUploaded
Pentobarbital SodiumACTIVE INGREDIENTNJJ0475N0S1
PentobarbitalACTIVE MOIETYI4744080IR1

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 3 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
0298-93720298-9372-68

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
Pentobarbital SodiumNJJ0475N0SACTIB

Source Document#

Source XML

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
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Pentobarbital SodiumPENTOBARBITAL SODIUMHikma Pharmaceuticals USA Inc.d375b92a-baa1-4d63-9ad1-1467dcfde7d52024-03-08Warnings, Adverse reactionsName fallback
generic name: PENTOBARBITAL SODIUM

Reported adverse events (FAERS/openFDA)#

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