Heparin Sodium Injection, Solution
Product Images NDC 81565-203

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 81565-203). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phlow Corporation, 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

FDA Label Image

Structure Of Heparin Sodium (Hep0w 0000 01)

Structure Of Heparin Sodium (Hep0w 0000 01)
Chemical structure diagram showing five numbered molecular units connected in sequence, representing a portion of the active ingredient Heparin Sodium. The structure includes sugar rings with hydroxyl, sulfate, and other functional groups, typical of heparin polysaccharide chains.*
FDA Label Image

Phlow Logo (Hep0w 0000 02)

Phlow Logo (Hep0w 0000 02)
FDA Label Image

Package Label – Principal Display Panel – Heparin 10 mL Multiple Dose Vial Label (Hep0w 0000 03)

Package Label – Principal Display Panel – Heparin 10 mL Multiple Dose Vial Label (Hep0w 0000 03)
Label for Heparin Sodium Injection, USP by Phlow Corporation showing a 10 mL vial containing 10,000 USP units total (1,000 USP units per mL). The label indicates the solution is for intravenous or subcutaneous use. Storage instructions and manufacturing details are present along with barcode and lot/expiration fields.*
FDA Label Image

Package Label – Principal Display Panel – Heparin 10 mL Multiple Dose Tray Label (Hep0w 0000 04)

Package Label – Principal Display Panel – Heparin 10 mL Multiple Dose Tray Label (Hep0w 0000 04)
Heparin Sodium Injection, USP 10,000 units per 10 mL (1,000 USP units per mL) multiple dose vial label by Phlow Corporation. The label states intravenous or subcutaneous use and contains 25 vials. It includes warnings about latex, sterility, and storage instructions, with a barcode and NDC 81565-203-02.*

* 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.