Chemical Structure (Fentanyl Citrate Injection Usp Novaplus 1)
Fentanyl Citrate Injection
Product Images NDC 0641-6290
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Fentanyl Citrate (NDC 0641-6290). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Hikma Pharmaceuticals Usa 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.
Unit Label (Fentanyl Citrate Injection Usp Novaplus 2)
This text contains information about a Fentanyl Citrate Injection, USP, with a recommended dosage of 400 micrograms per 2mL for intravenous or intramuscular use. It emphasizes protection from light and advises to discard any unused portion. The product comes in a 2mL single-dose vial manufactured by Hikma under the brand "novaplus." It also includes important identification numbers such as NDC (0641-6288-01) and a lot number for tracking purposes.*
Carton Label (Fentanyl Citrate Injection Usp Novaplus 3)
Unit Label (Fentanyl Citrate Injection Usp Novaplus 4)
This text contains information regarding a single dose of an injection product. The specific product is a Citrate Injection, USP. The recommended usual dosage is mentioned for intravenous use. The text also includes details such as NDC number and instructions for handling and disposing of the unused portion of the product. Additional details may not be available due to the text quality.*
Carton (Fentanyl Citrate Injection Usp Novaplus 5)
This is a product description for Fentanyl Citrate Injection, USP in a 20mL Single Dose Vial. The medication contains fentanyl citrate equivalent to 50mg fentanyl base per mL. It is indicated for slow intravenous use by hospital personnel trained in the use of narcotic analgesics. The solution is preservative-free and should be discarded if unused. For complete prescribing information, refer to the packaging insert. It is manufactured by Hi-Tech Pharmacal Co., Inc. in Berkeley Heights, NJ.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
