Butorphanol Tartrate Spray
Product Images NDC 72162-2099

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Butorphanol Tartrate (NDC 72162-2099). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Figure1.jpg (Figure1)

An instructional illustration showing a person holding a tissue over their nose and mouth, presumably demonstrating proper technique for using a nasal spray device or managing nasal discharge.*

FDA Label Image

Figure2.jpg (Figure2)

An illustration showing the assembly of a nasal spray device for Butorphanol Tartrate 10 mg/mL. The image depicts the positioning and attachment of the spray actuator onto the main spray bottle. Arrows indicate the direction of assembly steps.*

FDA Label Image

Figure3.jpg (Figure3)

An instructional diagram illustrating a hand holding and using a nasal spray device. The image highlights proper grip and positioning for administering the spray, consistent with the Butorphanol Tartrate nasal spray dosage form.*

FDA Label Image

Figure4.jpg (Figure4)

An instructional illustration depicting a person drinking from a cup with a straw. The image focuses on the hands holding the cup and the face, showing the person consuming a liquid through the straw. The illustration is likely intended to support usage directions for an oral medication or related administration instructions.*

FDA Label Image

Figure5.jpg (Figure5)

An instructional illustration showing a person administering nasal spray using one nostril, with the other hand holding a measuring cup or container. The image demonstrates the proper technique of nasal spray usage.*

FDA Label Image

Figure6.jpg (Figure6)

An instructional illustration showing a person using a nasal spray device. The person is depicted with the spray nozzle positioned inside the nostril, demonstrating the correct method for administering the spray.*

FDA Label Image

Figure7.jpg (Figure7)

An illustration of a person's profile demonstrating the correct nasal spray administration technique, with the spray aimed into the nostril while the head is tilted slightly back. This instructional image supports proper use of Butorphanol Tartrate nasal spray.*

FDA Label Image

Figure.jpg (Figure)

A pharmacokinetic line graph showing plasma concentration (ng/mL) over time (hours) for Butorphanol Tartrate administered via intravenous (IV), nasal spray (NS), and intramuscular (IM) routes. The graph displays mean concentration values with error bars for each time point up to 12 hours.*

FDA Label Image

Label (Lbl721622099)

Butorphanol Tartrate Nasal Spray, USP 10 mg/mL in a 2.5 mL container. The label includes the NDC 72162-2099-2, states it is for nasal use only, and notes the product is relabeled by Bryant Ranch Prepack, Inc. and manufactured by Apotex Inc. Storage instructions specify 20° to 25°C.*

FDA Label Image

Structure.jpg (Structure)

Chemical structure diagrams showing the molecular arrangement of butorphanol tartrate and tartaric acid, the active ingredient in Butorphanol Tartrate nasal spray 10 mg/mL by Bryant Ranch Prepack.*

FDA Label Image

Image Description (Symbol)

Butorphanol Tartrate 10 mg/mL nasal spray packaging label from Bryant Ranch Prepack. The label features the product name prominently with details including its strength and dosage form. The label also includes the National Drug Code (NDC) 72162-2099 and indicates it is a human prescription drug.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.