Potassium Phosphates Injection
Product Images NDC 70121-1722

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Potassium Phosphates (NDC 70121-1722). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Llc, 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

1 (Potassium Phosphates In Sodium Chloride Injection 1)

Label for Potassium Phosphates in 0.9% Sodium Chloride Injection, an intravenous injection supplied in a 250 mL single-dose container. Each mL contains 4.48 mg monobasic potassium phosphate and 4.72 mg dibasic potassium phosphate. Manufactured by Amneal Pharmaceuticals Pvt. Ltd and distributed by Amneal Pharmaceuticals LLC.*

FDA Label Image

1 (Potassium Phosphates In Sodium Chloride Injection 2)

Label of Potassium Phosphates in 0.9% Sodium Chloride Injection, an intravenous injection by Amneal Pharmaceuticals LLC. Contains 4.48 mg/mL Monobasic Potassium Phosphate and 4.72 mg/mL Dibasic Potassium Phosphate in a 250 mL single-dose container. Provides phosphorus 15 mmol/250 mL and potassium 22 mEq/250 mL. Includes storage instructions and manufacturer details.*

FDA Label Image

1 (Potassium Phosphates In Sodium Chloride Injection 3)

Label for Potassium Phosphates injection in 0.9% sodium chloride, supplied by Amneal Pharmaceuticals LLC. The label details strength with Phosphorus 15 mmol/250 mL and Potassium 22 mEq/250 mL. It is for intravenous infusion, packaged as 24 single-dose 250 mL containers. Storage and manufacturing information is included along with barcodes and regulatory data.*

* 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.