NDC 0298-9373-68 - Fatal-Plus Solution

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: 0298-9373
Requested NDC: 0298-9373-68
Package NDCs from labels: 0298-9373-68
Manufacturer: Vortech Pharmaceuticals, Ltd. | Vortech Pharmaceuticals, Ltd | Siegfried USA, LLC
Effective date: 2016-12-21
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Fatal-Plus Solution - Vortech Pharmaceuticals, Ltd. \| Vortech Pharmaceuticals, Ltd \| Siegfried USA, LLC	Vortech Pharmaceuticals, Ltd. \| Vortech Pharmaceuticals, Ltd \| Siegfried USA, LLC	2016-12-21	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
0298-9373-68	Fatal-Plus Solution	250 mL in 1 VIAL, MULTI-DOSE	INJECTION, SOLUTION	250		2

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
0298-9373	FATAL-PLUS SOLUTION (PENTOBARBITAL SODIUM) INJECTION, SOLUTION [VORTECH PHARMACEUTICALS, LTD.]	2	1 package rows	20161221_0da20b0f-dda7-47cb-917f-1d0002f0bcd7.zip

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
Pentobarbital Sodium	ACTIVE INGREDIENT	NJJ0475N0S	FATAL-PLUS SOLUTION (PENTOBARBITAL SODIUM) INJECTION, SOLUTION [VORTECH PHARMACEUTICALS, LTD.]	1
Pentobarbital	ACTIVE MOIETY	I4744080IR	FATAL-PLUS SOLUTION (PENTOBARBITAL SODIUM) INJECTION, SOLUTION [VORTECH PHARMACEUTICALS, LTD.]	1

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
Pentobarbital Sodium	PENTOBARBITAL SODIUM	Hikma Pharmaceuticals USA Inc.	d375b92a-baa1-4d63-9ad1-1467dcfde7d5	2024-03-08	Warnings, Adverse reactions	Exact identifier unii: NJJ0475N0S

Reported adverse events (FAERS/openFDA)#

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