Heparin Sodium In Sodium Chloride Injection, Solution
Product Images NDC 51662-1578

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Heparin Sodium In Sodium Chloride (NDC 51662-1578). 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

Bag Labeling (Bag Label)

Bag Labeling (Bag Label)
Label for Heparin Sodium in 0.45% Sodium Chloride Injection showing strength of 25,000 USP units per 250 mL (100 USP units per mL). Active ingredients include Heparin Sodium 10,000 USP units per 100 mL and Sodium Chloride 0.45 g. The label details storage conditions, cautions, and manufacturing information by Fresenius Kabi, made in Norway.*
FDA Label Image

Dosage (Dosage)

Dosage (Dosage)
A dosing table for Heparin Sodium in Sodium Chloride injection solution showing recommended doses by method of administration, including intermittent intravenous injection and continuous intravenous infusion, with frequencies and specific unit ranges for initial and ongoing doses.*
FDA Label Image

3 (Highlight 3)

3 (Highlight 3)
A text panel with a table listing the administration method 'Intravascular via Extracorporeal Dialysis' and an instruction to 'Follow equipment manufacturer's operating directions carefully.' This appears related to usage directions or precautions for the drug.*
FDA Label Image

Hs1 (Hs 1)

Hs1 (Hs 1)
A data table listing product codes, units of sale, strengths, and packaging details for two Heparin Sodium injection products. It shows 25,000 USP units per 500 mL and 25,000 USP units per 250 mL strengths, each sold in units of 24 with corresponding NDC numbers and single dose freeflex® bags.*
FDA Label Image

Hs2 (Hs 2)

Hs2 (Hs 2)
A table presenting product codes, units of sale, strengths, and package NDCs for HEPARIN SODIUM IN SODIUM CHLORIDE injection. It details two strengths: 25,000 USP units per 500 mL (50 USP/mL) and 25,000 USP units per 250 mL (100 USP/mL), each sold in units of 24 and available as single-dose freeflex bags.*
FDA Label Image

1 (Highlights 1)

1 (Highlights 1)
A dosing table for Heparin Sodium in Sodium Chloride injection showing initial and continuous doses for intermittent intravenous injection and continuous intravenous infusion. Dosages include 10,000 units initial dose and 5,000 to 10,000 units every 4 to 6 hours for intermittent injection, and 5,000 units initial with 20,000 to 40,000 units over 24 hours for continuous infusion, based on a 150 lb (68 kg) patient.*
FDA Label Image

2 (Highlights 2)

2 (Highlights 2)
A data table showing dosing information for HEPARIN SODIUM IN SODIUM CHLORIDE injection. It includes columns for administration method (Intravascular via Total Body Perfusion), initial dose, and specifics indicating an initial dose of at least 150 units per kilogram with adjustments for longer procedures.*
FDA Label Image
FDA Label Image

Serialized Labeling (Serialized Labeling)

Serialized Labeling (Serialized Labeling)
Packaging label for Heparin Sodium in Sodium Chloride injection solution, showing a white label with black text including a barcode, QR code, and identifiers (01, 17, 21, 10) along with distribution information by HF Acquisition Co., LLC, Mukilteo, WA 98275, and indicating 'RX ONLY'.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram showing the polysaccharide chains and sulfation pattern of heparin sodium, labeled with numbers 1 through 5 below different saccharide units.*

* 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.