Potassium Phosphates Solution, Concentrate
Product Images NDC 80830-1692

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Potassium Phosphates (NDC 80830-1692). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Private Limited, 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 Injection Usp 1)

1 (Potassium Phosphates Injection Usp 1)
Chemical structure diagram of potassium phosphate, showing phosphate group bonded to hydroxyl and potassium atoms.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 10)

1 (Potassium Phosphates Injection Usp 10)
Packaging label for Potassium Phosphates Injection, USP, intravenous solution concentrate with strengths of Phosphorus 150 mEq/50 mL and Potassium 220 mEq/50 mL. The label indicates it is a pharmacy bulk package, not for direct infusion, requiring dilution. Manufactured by Puniska Healthcare Pvt. Ltd., a subsidiary of Amneal Pharmaceuticals Private Limited, and distributed by Amneal Pharmaceuticals LLC.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 11)

1 (Potassium Phosphates Injection Usp 11)
Potassium Phosphates Injection, USP solution concentrate for intravenous use, labeled with phosphorus 150 mmol/50 mL (3 mmol/mL) and potassium 220 mEq/50 mL (4.4 mEq/mL). The label states it is a pharmacy bulk package not for direct infusion and must be diluted. Pack contains 10 x 50 mL vials. Manufactured by Puniska Healthcare Pvt. Ltd., distributed by Amneal Pharmaceuticals LLC.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 12)

1 (Potassium Phosphates Injection Usp 12)
This image shows multiple small rectangular labels arranged in a grid, each labeled 'Discard after' with blank lines for entering a discard date and time. The labels have alternating white and blue backgrounds for the date and time fields, designed for recording disposal information. No specific product branding or active ingredient information is visible.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 13)

1 (Potassium Phosphates Injection Usp 13)
A sheet of discard-after labels for intravenous solutions, each containing fields to fill in a discard date and time. The labels have a white background with a blue band highlighting the date and time entry spaces. No specific product branding or strength details are visible on the labels themselves.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 2)

1 (Potassium Phosphates Injection Usp 2)
Chemical structure diagram of potassium phosphate showing phosphorus atom bonded to oxygen and hydroxyl groups with potassium ions attached.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 3)

1 (Potassium Phosphates Injection Usp 3)
Label for Potassium Phosphates Injection, USP 236 mg/mL and 224 mg/mL solution concentrate for intravenous use. Provides phosphorus 15 mmol/5 mL and potassium 22 mEq/5 mL. Packaged as a 5 mL single-dose vial. Manufactured by Amneal Pharmaceuticals Private Limited, made in India. Includes caution that product must be diluted and for intravenous use only.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 4)

1 (Potassium Phosphates Injection Usp 4)
Carton label for Potassium Phosphates Injection, USP, a solution concentrate for intravenous use. The label highlights phosphorus 15 mmol/5 mL (3 mmol/mL) and potassium 22 mEq/5 mL (4.4 mEq/mL) contents. Packaging is by Amneal Pharmaceuticals Private Limited, containing 25 single-dose 5 mL vials. The label includes dilution caution and storage instructions.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 5)

1 (Potassium Phosphates Injection Usp 5)
Packaging label for Potassium Phosphates Injection, USP, a concentrated intravenous solution. Each 5 mL contains phosphorus 15 mmol and potassium 22 mEq. Supplied as 5 single-dose 5 mL vials. The label emphasizes the product must be diluted prior to intravenous use. Manufactured by Puniska Healthcare Pvt. Ltd., a subsidiary of Amneal Pharmaceuticals Private Limited.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 6)

1 (Potassium Phosphates Injection Usp 6)
Potassium Phosphates Injection USP solution concentrate in a 15 mL single-dose vial. It contains phosphorus 45 mmol/15 mL (3 mmol/mL) and potassium 66 mEq/15 mL (4.4 mEq/mL). The label notes the product is sterile, nonpyrogenic, preservative-free, for intravenous use only, and must be diluted before use. It is manufactured by Amneal Pharmaceuticals Private Limited.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 7)

1 (Potassium Phosphates Injection Usp 7)
Potassium Phosphates Injection, USP solution concentrate, featuring phosphorus 45 mmol/15 mL (3 mmol/mL) and potassium 66 mEq/15 mL (4.4 mEq/mL). The label indicates it is for intravenous use only, must be diluted, and includes 25 single-dose 15 mL vials. Manufactured by Puniska Healthcare Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 8)

1 (Potassium Phosphates Injection Usp 8)
Potassium Phosphates Injection, USP solution concentrate for intravenous use contains phosphorus 45 mmol/15 mL (3 mmol/mL) and potassium 66 mEq/15 mL (4.4 mEq/mL). The label indicates it is distributed by Amneal Pharmaceuticals LLC and manufactured by Puniska Healthcare Pvt. Ltd. The package contains 10 single-dose 15 mL vials and includes warnings that it is for intravenous use only and must be diluted before use.*
FDA Label Image

1 (Potassium Phosphates Injection Usp 9)

1 (Potassium Phosphates Injection Usp 9)
Potassium Phosphates Injection, USP, solution concentrate for intravenous use, labeled with phosphorus 150 mmol/50 mL and potassium 220 mEq/50 mL. The 50 mL pharmacy bulk package is for intravenous use only, marked with caution that it must be diluted before use. Distributed by Amneal Pharmaceuticals LLC, made in India, with storage instructions and product usage details.*

* 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.