NDC 0859-2395 - 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
0859-2395
Package NDCs from labels
0859-2395-02, 0859-2395-03
Manufacturer
Bayer HealthCare LLC, Animal Health Division
Effective date
2021-11-05
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
Butorphanol Tartrate - Bayer HealthCare LLC, Animal Health DivisionBayer HealthCare LLC, Animal Health Division2021-11-05PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Socrata Ingredients#

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 4 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Butorphanol TartrateBUTORPHANOL TARTRATEApotex Corp.b8e48063-0b40-ee43-85c1-4ef2de80c4042026-09-09Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2L7I72RUHN
Butorphanol TartrateBUTORPHANOL TARTRATEBryant Ranch Prepack412499ce-db93-4943-ae1a-564c27b1fb162026-03-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2L7I72RUHN
Butorphanol TartrateBUTORPHANOL TARTRATEHikma Pharmaceuticals USA Inc.5a50d22e-acbe-4b15-9ed6-70713378408a2025-11-20Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2L7I72RUHN
Butorphanol TartrateBUTORPHANOL TARTRATEHikma Pharmaceuticals USA Inc.bded5531-8847-4576-9a29-3e44f979d2e02024-04-11Boxed warning, Warnings, Adverse reactionsExact identifier
unii: 2L7I72RUHN

Reported adverse events (FAERS/openFDA)#

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