Heparin Sodium Injection
Product Images NDC 68083-428

3 FDA label images from Gland Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 68083-428). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma 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.

Product Images & Figures Index

FDA Label Image

Structure-image01 (Image01)

Structure-image01 (Image01)
Chemical structure diagram showing five saccharide units of the active ingredient Heparin Sodium. The structure illustrates key groups such as sulfate and hydroxyl substituents on the sugar rings, representing the complex polysaccharide nature of Heparin Sodium.*
FDA Label Image

Vial Label-image02 (Image02)

Vial Label-image02 (Image02)
Label for Heparin Sodium Injection, USP 5,000 USP units per mL, 1 mL dose. Intended for intravenous or subcutaneous use. Manufactured by Gland Pharma Limited in India. Includes NDC 68083-136-01 and warnings such as 'Not for lock flush.' Also shows space for lot and expiration details.*
FDA Label Image

Carton Label-image03 (Image03)

Carton Label-image03 (Image03)
Heparin Sodium Injection, USP 5000 USP units per mL packaging label for 25 vials of 1 mL each by Gland Pharma Limited. The label states the product is for intravenous or subcutaneous use, derived from porcine intestines, and includes storage instructions and regulatory information. The label prominently displays the dosage strength in an orange box and notes it is not for lock flush.*

* 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.