NDC 11695-7044-2 - Butorphanol Tartrate

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: 11695-7044
Requested NDC: 11695-7044-2
Package NDCs from labels: 11695-7044-1, 11695-7044-2
Manufacturer: Covetrus
Effective date: 2026-03-17
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Butorphanol Tartrate - Covetrus	Covetrus	2026-03-17	PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11695-7044-1	Butorphanol Tartrate	20 mL in 1 VIAL, MULTI-DOSE	INJECTION	20	1
11695-7044-1	Butorphanol Tartrate	1 in 1 CARTON	INJECTION	1	1
11695-7044-2	Butorphanol Tartrate	50 mL in 1 VIAL, MULTI-DOSE	INJECTION	50	1
11695-7044-2	Butorphanol Tartrate	1 in 1 CARTON	INJECTION	1	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 · 4 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Butorphanol Tartrate	BUTORPHANOL TARTRATE	Apotex Corp.	b8e48063-0b40-ee43-85c1-4ef2de80c404	2026-09-09	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 2L7I72RUHN
Butorphanol Tartrate	BUTORPHANOL TARTRATE	Bryant Ranch Prepack	412499ce-db93-4943-ae1a-564c27b1fb16	2026-03-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 2L7I72RUHN
Butorphanol Tartrate	BUTORPHANOL TARTRATE	Hikma Pharmaceuticals USA Inc.	5a50d22e-acbe-4b15-9ed6-70713378408a	2025-11-20	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 2L7I72RUHN
Butorphanol Tartrate	BUTORPHANOL TARTRATE	Hikma Pharmaceuticals USA Inc.	bded5531-8847-4576-9a29-3e44f979d2e0	2024-04-11	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 2L7I72RUHN

Reported adverse events (FAERS/openFDA)#

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