Heparin Sodium Injection, Solution
Product Images NDC 63323-118

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 63323-118). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Hepar-img-01.jpg (Hepar Img 01)

An instructional diagram showing the components of a prefilled syringe outer package. Labeled parts include the plunger rod, syringe barrel, label (marked Do not remove), syringe tip cap, and luer lock collar (marked Do not remove). The diagram provides clear identification of each part of the syringe used for injection.*

FDA Label Image

Hepar-img-02.jpg (Hepar Img 02)

Illustration depicting two hands opening a sealed blister pack containing a prefilled injection device, likely showing the initial step to access the Heparin Sodium injection solution for intravenous or subcutaneous administration.*

FDA Label Image

Hepar-img-03.jpg (Hepar Img 03)

An instructional illustration showing two hands opening a vial by twisting the cap. The image depicts the action of removing the vial cap in preparation for use.*

FDA Label Image

Hepar-struc-01.jpg (Hepar Struc 01)

Chemical structure diagram depicting five distinct sugar units as part of the Heparin Sodium molecule, illustrating the molecular framework of the active pharmaceutical ingredient.*

FDA Label Image

Hepar-img-04.jpg (Hepar Img 04)

FDA Label Image

Hepar-label-01.jpg (Hepar Label 01)

Label for Heparin Sodium Injection, USP 5000 USP units per 0.5 mL. The product is intended for intravenous or subcutaneous use and comes as 24 prefilled single-dose 0.5 mL syringes. It is derived from porcine intestinal mucosa and labeled not for lock flush use. The labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

Hepar-label-02.jpg (Hepar Label 02)

Label for Heparin Sodium Injection, USP 5000 USP units per 0.5 mL in a 0.5 mL prefilled single-dose syringe. The product is indicated for intravenous or subcutaneous use but is not for lock flush. The label includes storage instructions, dosage guidance referencing package insert, and barcode with lot and expiration placeholders. Manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

Hepar-label-03.jpg (Hepar Label 03)

Label of Heparin Sodium Injection, USP, 5,000 USP units per 0.5 mL prefilled single-dose syringe. For intravenous or subcutaneous use, sourced from porcine intestines. Label includes the caution 'NOT for lock flush,' manufacturer Fresenius Kabi, and a barcode with product identification numbers.*

* 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.