Butorphanol Tartrate Injection, Solution
Product Images NDC 0409-1623
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Butorphanol Tartrate (NDC 0409-1623). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hospira, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Product Images & Figures Index
Figure 1 (Butorphanol 02)
Hospira Logo (Butorphanol 03)
Principal Display Panel (2 mg/mL Vial Label)
This is a prescription drug with the name Butorphanol Tartrate Injection, USP. It is a single-dose medication, and the usual dosage is not mentioned. The drug is recommended for intramuscular or intravenous use, and it is distributed under the name RL-7142 by Hospira, Inc, located in Lake Forest, IL 60045, USA. The National Drug Code (NDC) for this drug is 0409-1626-21. The recommended storage temperature is 20 degrees Celsius.*
Principal Display Panel (2 mg/mL Vial Carton)
This is a description of a medication called CA7050. It is a single-dose injection that contains 2mg/mL of Butorphanol Tartrate. The medication is intended for intramuscular or intravenous use and is distributed by Hospira. The medication is nonpyrogenic and sterile, and it needs to be stored at a temperature of 20-25°C (68-77°F). Each mL of the medication contains butorphanol tartrate 2mg, sodium citrate dihydrate 6.4 mg, citric acid hydrous 3.3 mg, and sodium chloride 6.4 mg. The dosage for adults is usually 2mg intramuscular or 1 mg intravenous every three to four hours as required.*
Principal Display Panel (4 mg/2 mL Vial Label)
Principal Display Panel (4 mg/2 mL Vial Carton)
This is a product description for Butorphanol Tartrate injection, a medication used for intravenous or intramuscular use. It comes in a 2ml flip-top vial, with 4mg/2ml strength. Each mL contains Butorphanol tartrate 2mg, and is sodium chloride 6.4 mg. It is sterile and nonpyrogenic, and should be stored at 20-25°C. This medication should be protected from light. This product is manufactured by Hospir, In, and is distributed in the USA and Great Britain. Dosage should be taken as directed by a physician.*
Principal Display Panel (1 mg/mL Vial Label)
This is a description of a medication called BUTORPHANOL TARTRATE in an injectable form with a strength of 1mg/mL. The NDC number is 0409-1623-21, and it should be stored at a temperature of 25°C (77°F). The recommended dosage is available on the insert. It is distributed by Hospira, Inc. in Lake Forest, IL, USA. It is suitable for LM or LV use. The text also contains a random "HiH" at the end.*
Principal Display Panel (1 mg/mL Vial Carton)
This is a drug label for Butorphanol Tartrate Injection, USP, which contains 1mg/mL Butorphanol Tartrate, and is intended for Intramuscular or Intravenous use. The drug is sterile, non-pyrogenic, and should be discarded if any unused portion is left. The usual dosage for the drug is 2mg Intramuscular, or 1mg Intravenous use for adults, to be repeated every 3 to 4 hours as required. The drug should be protected from light, and should be stored at a temperature of 20 to 25°C. Use aseptic technique while handling the drug.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.