Heparin Sodium Injection, Solution
Product Images NDC 51662-1434

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 51662-1434). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

Dosage (Dosage)

A dosage regimen table for Heparin Sodium injection. It details methods of administration including deep subcutaneous injection, intermittent intravenous injection, and intravenous infusion, with corresponding frequencies and recommended doses for a 150 lb patient. The table covers initial and subsequent dosing ranges, intravenous solutions used, and administration intervals.*

FDA Label Image

How Supplied (How Supplied)

A table presenting NDC numbers, concentrations, vial fill volumes, vial types, and pack sizes for heparin sodium injection solutions. It lists multiple strengths from 1,000 to 20,000 USP units/mL, vial volumes ranging from 1 mL to 30 mL, all multiple dose vials, packaged in cartons of 25 vials.*

FDA Label Image

Serialized Vial Labeling (Serialized Vial Labeling)

HEPARIN SODIUM 10,000 USP Units/mL injection, solution vial labeled for intravenous and subcutaneous use. The label shows the proprietary name HEPARIN SODIUM INJECTION, USP, multiple dose vial, 1 mL, with a red safety cap and includes usage instructions and regulatory information. Distributed by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Structure (Structure)

Chemical structure diagram showing multiple sugar rings with functional groups, representing the molecular structure of the active ingredient heparin sodium.*

FDA Label Image

Vial Labeling (Vial Labeling)

Label for Heparin Sodium Injection USP 10,000 USP units/mL, multiple dose vial, 1 mL. Intended for intravenous or subcutaneous use. The label notes the product is derived from porcine intestinal mucosa, sterile, and nonpyrogenic. Storage recommended at 20 to 25°C (68 to 77°F). Manufactured in India for McKesson Corporation dba SKY Packaging. Includes barcodes and a warning: '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.