Heparin Sodium
Product Images NDC 0404-9873

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0404-9873). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Henry Schein, Inc., 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

Formula1.jpg (Formula1)

Chemical structure diagram showing multiple sugar rings and functional groups, representing the active ingredient in Heparin Sodium. The diagram includes five labeled sugar moieties with various hydroxyl, sulfate, acetyl, and carboxylate groups attached, illustrating the complex polysaccharide structure characteristic of heparin.*

FDA Label Image

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A dosing recommendation table for Heparin Sodium detailing method of administration, frequency, and recommended doses for a 150 lb (68 kg) patient. It includes deep subcutaneous injection, intermittent intravenous injection, and intravenous infusion with specific unit doses and frequency, highlighting use of solutions like 0.9% Sodium Chloride Injection, USP.*

FDA Label Image

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A dosing table for Heparin Sodium detailing initial doses (75-100 units/kg IV bolus over 10 minutes for general use, 25-30 units/kg/hour for infants, with infants under 2 months requiring about 28 units/kg/hour), maintenance doses (18-20 units/kg/hour for children over 1 year, with older children possibly needing less), and monitoring instructions to adjust dosage to maintain an APTT of 60-85 seconds, reflecting an anti-Factor Xa level of 0.35-0.70.*

FDA Label Image

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Table showing amounts of Sodium Chloride and Benzyl Alcohol corresponding to different strengths of Heparin Sodium: 1,000 USP units with 8.6 mg Sodium Chloride and 10.4 mg Benzyl Alcohol, 5,000 USP units with 7 mg Sodium Chloride and 10.4 mg Benzyl Alcohol, and 10,000 USP units with 5 mg Sodium Chloride and 10.4 mg Benzyl Alcohol.*

FDA Label Image

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This table lists NDC codes for HEPARIN SODIUM from Henry Schein, Inc., organized by dosage strength and vial count. It includes 1,000 USP units per mL, 5,000 USP units per mL, and 10,000 USP units per mL, each available as single-dose vials in 1 vial or 25 vial pack sizes.*

FDA Label Image

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A table listing vial sizes and NDC codes for Heparin Sodium by Henry Schein, Inc. It details different concentrations and package counts: 1,000 USP units per mL in 10 mL and 30 mL multi-dose vials; 5,000 USP units per mL in 10 mL vials; and 10,000 USP units per mL in 4 mL multi-dose vials, along with corresponding NDC numbers for each configuration.*

FDA Label Image

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HEPARIN SODIUM 10,000 USP units per ml injection label for a single dose vial. The label indicates use for intravenous or subcutaneous administration, with warnings against use as a lock flush and containing benzyl alcohol. Storage instructions specify 20 to 25°C (68 to 77°F). Packaged by Henry Schein, Inc., Bastian, Virginia. Includes NDC 0404-9873-01 and barcode.*

* 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.