Sodium Acetate 50 mL Vial Label (Sodium Acetate Injection Usp Pbp 1)
Sodium Acetate Injection
Product Images NDC 0641-6263
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Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sodium Acetate (NDC 0641-6263). 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.
Sodium Acetate 50 mL Pbp Carton (Sodium Acetate Injection Usp Pbp 2)
This text appears to contain information about a medication called Sodium Acetate Injection, USP. It provides details such as the concentration (100 mEq per 50 mL), directions for use (Pharmacy Bulk Pack for Direct Infusion), and a caution about the need for dilution before intravenous administration. Specific instructions are given for discarding the solution after 4 hours if not used. The text also includes some identification numbers (NDC 0541626201) and a manufacturer's information. This Sodium Acetate solution is intended for intravenous use only.*
Sodium Acetate 100 mL Vial Label (Sodium Acetate Injection Usp Pbp 3)
This text appears to be a label for a medication called Sodium Acetate Injection, USP. It provides information about the manufacturer (Hikma Pharmaceuticals USA Inc.), dosage (200 mEq per 100 mL), package type (Pharmacy Bulk Package), and instructions for use (not for direct infusion, must be diluted for intravenous use only). It also includes a caution statement and details on storage conditions. The text seems to be an important reference for healthcare professionals handling this medication.*
Sodium Acetate 100 mL Carton Label (Sodium Acetate Injection Usp Pbp 4)
This is a description of Sodium Acetate Injection, USP in a Pharmacy Bulk Package with each mL containing sodium acetate, anhydrous 164 mg. It is for intravenous use only and needs to be diluted before use. The package contains 10 x 100 mL vials and should be stored at 20° to 25°C. It is important to follow proper aseptic technique and use a sterile dispensing set or transfer device for administration. The product is manufactured by Hikma Pharmaceuticals USA Inc.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
