Potassium Phosphates Injection, Solution, Concentrate
Product Images NDC 68462-787

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Potassium Phosphates (NDC 68462-787). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glenmark Pharmaceuticals Inc., Usa, 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
FDA Label Image

Potassium-phosphates-carton-15ml (Potassium Phosphates Carton 15ml)

Potassium-phosphates-carton-15ml (Potassium Phosphates Carton 15ml)
Potassium Phosphates Injection, USP 45 mmol/15 mL phosphorus and 66 mEq/15 mL potassium in injection solution concentrate, labeled for intravenous use. The label states the product is sterile and must be diluted before intravenous use. Packaged as 25 single-dose vials of 15 mL each, distributed by Glenmark Pharmaceuticals Inc., USA. The label includes storage and ingredient details, a barcode, and caution notes.*
FDA Label Image

Potassium-phosphates-carton-50ml (Potassium Phosphates Carton 50ml)

Potassium-phosphates-carton-50ml (Potassium Phosphates Carton 50ml)
Potassium Phosphates Injection, USP label for 25 vials of 50 mL pharmacy bulk package solution concentrate. Contains phosphorus 150 mmol/50 mL and potassium 220 mEq/50 mL. Intended for intravenous use after dilution. Manufactured by Glenmark Pharmaceuticals Inc., USA. The label includes cautionary and storage instructions, and a visible barcode.*
FDA Label Image

Potassium-phosphates-carton-5ml (Potassium Phosphates Carton 5ml)

Potassium-phosphates-carton-5ml (Potassium Phosphates Carton 5ml)
Label for Potassium Phosphates Injection, USP by Glenmark Pharmaceuticals Inc., USA. The solution is provided as 25 single-dose vials of 5 mL each. Strength details include Phosphorus 15 mmol/5 mL (3 mmol/mL) and Potassium 22 mEq/5 mL (4.4 mEq/mL). The label includes caution for dilution and indicates use for intravenous administration only.*
FDA Label Image

Potassium-phosphates-container-15ml (Potassium Phosphates Container 15ml)

Potassium-phosphates-container-15ml (Potassium Phosphates Container 15ml)
Label for Potassium Phosphates Injection, USP, an intravenous solution concentrate by Glenmark Pharmaceuticals Inc., USA. The label indicates phosphate 45 mmol/15 mL and potassium 66 mEq/15 mL strengths, with a concentration of 224 mg/mL of phosphates. The product is supplied in a 15 mL single-dose vial for prescription use only. The label includes storage instructions, dilution warnings, and lot/expiration date fields.*
FDA Label Image

Potassium-phosphates-container-50ml (Potassium Phosphates Container 50ml)

Potassium-phosphates-container-50ml (Potassium Phosphates Container 50ml)
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 50 mL pharmacy bulk package is marked 'Not for Direct Infusion' and manufactured by Glenmark Pharmaceuticals Inc., USA. The label includes storage instructions, caution for dilution, and barcodes.*
FDA Label Image

Potassium-phosphates-container-5ml (Potassium Phosphates Container 5ml)

Potassium-phosphates-container-5ml (Potassium Phosphates Container 5ml)
Label for Potassium Phosphates Injection, USP, manufactured by Glenmark Pharmaceuticals Inc., USA. It is a 5 mL single-dose vial of intravenous injection concentrate containing phosphorus 15 mmol/5 mL (3 mmol/mL) and potassium 22 mEq/5 mL (4.4 mEq/mL). The label emphasizes that the product must be diluted before use and includes storage and handling instructions.*

* 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.