Structural Formula (Phenylephrine Hydrochloride Injection Usp Nda 1)
Immphentiv Injectable, Liposomal
Product Images NDC 0641-6246
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Product Visual Gallery
This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Immphentiv (NDC 0641-6246). 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.
Product Images & Figures Index
West-ward Logo (Phenylephrine Hydrochloride Injection Usp Nda 2)
This is a description for Phenylephrine HCI Injection, a medication to be used intravenously. It contains 10mg/mL and comes in a 1 mL single-dose vial. The medication should be diluted before use and protected from light. The manufacturer is identified as M4 by Hikma. The National Drug Code (NDC) is listed as 0641-6142-01.*
Ndc 0641-6142-01 Phenylephrine HCl Injection, Usp 10 mg/ml For Intravenous Use Dilute Before Use 1 mL Single Dose Vial Discard Unused Portion Protect From Light (Phenylephrine Hydrochloride Injection Usp Nda 3)
Lor Phenylephrine HCI Injection, USP is an intravenous drug presented as 10mg/mL in a 26-packs of 1mL single-dose vials. It is advised to dilute the drug prior to use and discard any remaining fluid. The drug contains Pheny oride, Sodum Chiorde, Sodiu Gite, Diydrate, Ciic Acid Monobydiate, Sodium Metabisuifte and Water for injection. It is important to protect the drug from light and store it at room temperature. The manufacturer is Hikma, and the NDC is 0641-6142-25.*
Ndc 0641-6142-25 Rx Only Phenylephrine HCl Injection, Usp 10 mg/ml For Intravenous Use Dilute Before Use 25 X 1 mL Single Dose Vials Discard Unused Portion (Phenylephrine Hydrochloride Injection Usp Nda 4)
Phenylephrine HC Injection is a medication for intravenous use. Its presentation is 50 mg/5 mL (10 mg/mL). The rest of the text seems to be non-sense and does not provide any useful information. Therefore, the complete description for this text is: "Phenylephrine HC Injection is a medication for intravenous use. Its presentation is 50 mg/5 mL (10 mg/mL).".*
Phenylephrine Hydrochloride Injection Usp Nda 5
Phenylephrine HCI Injection, USP is a Pharmacy Bulk Package for Intravenous use, which needs to be diluted and protected from light. It contains Phenylephrine Hydrochloride, Sodium Chloride, Sodium Gtrate Dinydrate, Citric Acid Monohydrate, Sodium Metabisufft, and Water for Injection. It should be stored at 20° to 25°C and used within 4 hours. Detailed information can be found in the Package Inser. Manufactured in the United States.*
Phenylephrine Hydrochloride Injection Usp Nda 6
This is a description of a medication called Phenylephrine that comes in an injected form. It must be adjusted with other substances to have a pH of 30.65 and be used within 48 hours of opening the vial. It should be stored at a temperature between 20°C and 25°C. The medication comes in a 10 mL vial and must be diluted before use. It is not clear what the medication is used for.*
Phenylephrine Hydrochloride Injection Usp Nda 7
This is a description of a Pharmacy Bulk Package of Phenylephrine HCI Injection, USP, containing 100mg/10mL (10mg/mL) which is not for direct infusion but for intravenous use only. The package includes 10x10mL vials that must be diluted and protected from light, stored in the carton until use. The solution contains Phenylephrine Hydrochloride 10 mg, Sodium Chloride 35 mg, Sodium Grate Dihydrate 4 mg, Gtrc Acid Monohydate 1 mg, Sogium Metabisift 2 mg, with Water for Injection and pH adjusted with Sodium Hydroxide and/or Hydrochloric Acid. The solution must be stored at 20° to 25°C (68° to 77°F) and dispensed from the bulk vial within 4 hours after it is penetrated. The manufacturer is Hikma and the product is made in the USA.*
Phenylephrine Hydrochloride Injection Usp Nda 8
This text contains product identification information such as the GTIN (Global Trade Item Number), the SN (Serial Number), the expiration date, and the LOT number.*
* 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.
