FDA.reportPublic FDA data

NDC 11695-7044 - 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
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
LabelManufacturerEffective dateType
Butorphanol Tartrate - CovetrusCovetrus2026-03-17PRESCRIPTION ANIMAL DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
11695-7044-1Butorphanol Tartrate20 mL in 1 VIAL, MULTI-DOSEINJECTION201
11695-7044-1Butorphanol Tartrate1 in 1 CARTONINJECTION11
11695-7044-2Butorphanol Tartrate50 mL in 1 VIAL, MULTI-DOSEINJECTION501
11695-7044-2Butorphanol Tartrate1 in 1 CARTONINJECTION11