Heparin Sodium Injection, Solution
Product Images NDC 51662-1409

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 51662-1409). 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 dosing table for Heparin Sodium injection, solution showing methods of administration (Deep Subcutaneous Injection, Intermittent Intravenous Injection, Intravenous Infusion), frequency (Initial Dose, Every 8 hours, Every 12 hours, Every 4 to 6 hours, Continuous), and recommended doses for a 150 lb patient in units and solution concentrations.*

FDA Label Image

How Supplied 1 (How Supplied 1)

A data table listing two Heparin Sodium injection products with details on product number, NDC number, strength, and fill volume. The first product has 2,000 USP Heparin units per 2 mL (1,000 USP units/mL) with 2 mL fill volume in a single-dose flip-top vial, package of 25. The second product has 5,000 USP Heparin units per 0.5 mL with 0.5 mL fill volume in a single-dose flip-top vial, package of 25.*

FDA Label Image

How Supplied 2 (How Supplied 2)

A table presenting information on Heparin Sodium injection products. It lists product numbers, NDC codes, strengths including USP Heparin units per mL, and fill volumes in multi-dose, flip-top vials with package sizes. Two products are detailed: one with 50,000 USP Heparin units per 10 mL in 10 mL vials, and another with 40,000 USP Heparin units per 4 mL in 5 mL vials.*

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How Supplied 3 (How Supplied 3)

A data table listing multiple Heparin USP products with product numbers, NDC numbers, strengths in USP Heparin units per mL or per total volume, and corresponding fill volumes with vial sizes. Strengths range from 1,000 to 50,000 USP Heparin units with various vial fill volumes from 1 mL to 30 mL.*

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Logo (Logo)

FDA Label Image

Serialized Label Ndc 51662 1409 1 March 2021

A barcode label for Heparin Sodium injection solution, distributed by HF Acquisition Co LLC, DBA HealthFirst, Mukilteo, WA. The label contains Data Matrix barcode and human-readable codes including GTIN, lot number, and expiration date. It indicates prescription use and refers to manufacturer's package insert for details.*

FDA Label Image

Serialized Vial (Serialized Vial)

Vial of Heparin Sodium Injection, USP 50,000 units per 5 mL (10,000 USP units per mL) for intravenous or subcutaneous use. The vial has a brown cap and a brown label with white text listing the product name and strength. A secondary label with a QR code and manufacturing information is partially visible. Distributed by HF Acquisition Co LLC, DBA HealthFirst.*

FDA Label Image

Structure (Structure)

Chemical structure diagram showing multiple sugar units labeled 1 through 5, representing the molecular structure of the active ingredient heparin sodium.*

FDA Label Image

Vial Label Ndc 51662 1409 1 March 2021 Update

Label for Heparin Sodium Injection, USP showing a strength of 50,000 USP units per 5 mL (10,000 units per mL). The label indicates suitability for intravenous or subcutaneous use and includes a warning that it is not for lock flush. Manufacturer listed as Fresenius Kabi USA, with storage instructions to keep at 20 to 25°C (68° to 77°F). Barcode and lot/expiration fields visible.*

FDA Label Image

Vial Label (Vial Label)

Label for Heparin Sodium Injection, USP 50,000 units per 5 mL (10,000 units per mL) solution. The label indicates the product is for intravenous or subcutaneous use and includes a caution that it is not for lock flush. Manufactured by Fresenius Kabi USA, LLC, it also shows storage instructions and a 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.