Heparin Sodium Injection, Solution
Product Images NDC 51662-1486

Product Visual Gallery

This gallery contains 12 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 51662-1486). 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

Alternate Vial Label (Alternate Vial Label)

Label for Heparin Sodium Injection, USP 10,000 USP Units/mL, 1 mL single-dose vial. The label indicates the product is for intravenous or subcutaneous use, contains preservative, and is distributed by Hospira, Inc. It prominently states "NOT for LOCK FLUSH" repeatedly in red and white text.*

FDA Label Image

Description (Description Table)

A data table comparing amounts of Sodium Chloride and Benzyl Alcohol in solutions of Heparin Sodium at different strengths: 1,000 USP units, 5,000 USP units, and 10,000 USP units. Sodium Chloride ranges from 8.6 mg to 5 mg, Benzyl Alcohol remains constant at 0.01 mL.*

FDA Label Image

Dosage 1 (Dosage 1)

A data table titled 'Recommended Adult Full-Dose Heparin Regimens for Therapeutic Anticoagulant Effect' outlining methods of administration, frequency, and recommended doses of Heparin Sodium for adult patients. It includes dosing information for Deep Subcutaneous Injection, Intermittent Intravenous Injection, and Intravenous Infusion with specified unit doses and administration notes.*

FDA Label Image

Dosage 2 (Dosage 2)

This text panel provides dosing information for Heparin Sodium injection. It details the initial dose as 75 to 100 units/kg by IV bolus over 10 minutes, maintenance doses for infants and children by weight and age, and guidance on monitoring heparin therapy by adjusting to maintain specific aPTT and anti-Factor Xa levels.*

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Highlight 2 (Highlight 2)

A table listing preserved Heparin Sodium injection vial strengths with benzyl alcohol. Single-dose vials include 1,000, 5,000, and 10,000 USP units/mL per 1 mL vial. Multiple-dose vials include 1,000 USP units/mL with 10 mL and 30 mL vial sizes, and 5,000 USP units/mL with a 10 mL vial size.*

FDA Label Image

Highlight 1 (Highlights 1)

A dosage instruction table for Heparin Sodium injection, solution, detailing therapeutic anticoagulant doses based on administration method: Deep Subcutaneous Injection, Intermittent Intravenous Injection, and Intravenous Infusion. It includes initial and maintenance doses with units and solution concentration guidelines, emphasizing dose adjustments based on patient weight and laboratory monitoring.*

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How Supplied (How Supplied)

This table lists various NDC codes and packaging options for Heparin Sodium Injection, USP, showing unit of sale, concentration in USP Units per mL or per 10 mL, and vial types including 1 mL single-dose vials and multi-dose vials of 10 mL and 30 mL in trays of 25 units.*

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Logo (Logo)

FDA Label Image

Serialized Vial Labeling (Serialized Vial)

HEPARIN SODIUM 10,000 USP Units/mL injection, solution in a 1 mL single-dose vial. The vial label shows the product name, strength, and administration route as sodium injection USP. A red band on the vial cap and lower label states NOT for LOCK FLUSH. The labeler is HF Acquisition Co LLC, DBA HealthFirst. The vial is accompanied by a label with a barcode and serialized numeric codes.*

FDA Label Image

Structure (Structure)

Chemical structure diagram showing a polysaccharide chain representing Heparin Sodium. The structure includes five connected sugar rings with various functional groups such as sulfate (OSO3-), hydroxyl (OH), carboxylate (COO-), and acetyl (NHAc) groups attached, illustrating the molecular composition of Heparin Sodium.*

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Superseeded Vial Label (Superseeded Vial Label)

HEPARIN Sodium Injection, USP 10,000 USP Units/mL in a 1 mL single-dose vial. The label highlights it is not for lock flush use. It is intended for intravenous or subcutaneous use and contains preservative, sourced from porcine intestines. Labeler is Hospira, Inc., Lake Forest, IL.*

FDA Label Image

Vial Label (Vial Label)

HEPARIN SODIUM 10,000 USP units per mL injection solution label from HF Acquisition Co LLC, DBA HealthFirst. The label specifies a 1 mL single-dose vial for intravenous or subcutaneous use and prominently states 'NOT for LOCK FLUSH' in red panels. Contains standard product and lot information areas.*

* 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.