Heparin Sodium Injection, Solution
Product Images NDC 63323-915

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 63323-915). 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

Structure Of Heparin Sodium (Hep0l 0005 01)

Chemical structure diagram showing five distinct molecular components labeled 1 through 5, representing the complex molecular structure of heparin sodium.*

FDA Label Image

Fresenius Kabi Logo (Hep0l 0005 02)

FDA Label Image

504001 (Hep0l 0005 03)

Heparin Sodium Injection USP label from Fresenius Kabi USA, LLC. It displays a strength of 1,000 USP units per mL in a 1 mL volume. The label includes warnings stating "NOT FOR LOCK FLUSH" in yellow and black, along with usage instructions for intravenous or subcutaneous administration. The NDC number 63323-540-03 is visible.*

FDA Label Image

504001 (Hep0l 0005 04)

Heparin Sodium Injection, USP label for 1,000 USP units per mL strength in a 1 mL vial. The label indicates it is for intravenous or subcutaneous use and comes in a pack of 25 vials. The labeler is Fresenius Kabi USA, LLC. The label includes instructions for use, storage conditions, and cautions such as 'Not For Lock Flush.'*

FDA Label Image

926201 (Hep0l 0005 05)

Heparin Sodium Injection USP label for 5000 USP units per mL strength in a 1 mL vial. The label includes directions for intravenous or subcutaneous use, with a warning that the product is not for lock flush. Labeler is Fresenius Kabi USA, LLC. The label also notes the vial is for multiple doses and for porcine intestinal mucosa origin.*

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926201 (Hep0l 0005 06)

Heparin Sodium Injection, USP 5000 USP units per mL, 1 mL multiple dose vial carton containing 25 vials. Label states it is for intravenous or subcutaneous use and not for lock flush. Manufactured by Fresenius Kabi USA, LLC with storage instructions and inactive ingredients listed.*

FDA Label Image

504201 (Hep0l 0005 07)

Label for Heparin Sodium Injection, USP 10,000 USP units per mL in a 1 mL multiple dose vial. The label includes administration instructions for intravenous or subcutaneous use and highlights 'NOT FOR LOCK FLUSH' in yellow and black. The product is labeled by Fresenius Kabi USA, LLC with NDC 63323-542-09.*

FDA Label Image

504201 (Hep0l 0005 08)

Heparin Sodium Injection, USP 10,000 USP units per mL in a 1 mL multiple-dose vial. The label includes usage instructions for intravenous or subcutaneous use and states that the product contains preservatives. Packaged in a box with 25 vials. Manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

504509 (Hep0l 0005 09)

Label for Heparin Sodium Injection, USP, 40,000 USP units per 4 mL (10,000 USP units per mL) by Fresenius Kabi USA, LLC. The label includes a warning that the product contains benzyl alcohol, cautioning it is not for lock flush use. Directions and storage instructions are printed alongside the product name, strength, volume, and barcode.*

FDA Label Image

504509 (Hep0l 0005 10)

Heparin Sodium Injection, USP label for 40,000 USP units per 4 mL (10,000 USP units per mL) strength. The label indicates the product is for intravenous or subcutaneous use and comes in a package of 25 vials. It includes a warning regarding benzyl alcohol and dosing instructions. The labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

915501 (Hep0l 0005 11)

Label for Heparin Sodium Injection USP, 20,000 USP units per mL, in a 1 mL dosage form. The label cautions 'NOT FOR LOCK FLUSH' and states it is for intravenous or subcutaneous use. It is from Fresenius Kabi USA, LLC, with a multiple dose vial containing porcine intestinal mucosa-derived heparin. The label includes the NDC 63323-915-03 and a barcode.*

FDA Label Image

915501 (Hep0l 0005 12)

Heparin Sodium Injection, USP 20,000 USP units per mL label for a 1 mL multiple dose vial with 25 vials per carton. The label states it is for intravenous or subcutaneous use and is made by Fresenius Kabi USA, LLC. It contains detailed ingredient and storage information and a note that it is not for lock flush.*

FDA Label Image

504302 (Hep0l 0005 13)

Label for Heparin Sodium Injection, USP, showing 5,000 USP units per 0.5 mL in preservative-free solution. The label includes a warning "NOT FOR LOCK FLUSH" in yellow and black sections, and states it is for IV or SC use. The labeler is Fresenius Kabi USA, LLC, with NDC 63323-543-03 and a barcode visible on the right.*

FDA Label Image

504302 (Hep0l 0005 14)

Heparin Sodium Injection USP 5,000 USP units per 0.5 mL single dose vial, 25 vials per package. The label indicates intravenous or subcutaneous use, preservative free. Manufactured by Fresenius Kabi USA, LLC, with instructions noting it is not for lock flush and is made from porcine intestinal mucosa.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Heparin Sodium Injection, USP label for 10,000 USP units per 10 mL (1,000 USP units per mL) in a vial. The label includes usage information for intravenous or subcutaneous use, storage instructions at 20°C to 25°C (68°F to 77°F), and indicates it is provided by Fresenius Kabi USA, LLC. It also states the product is not for lock flush.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Label for Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) in a multiple dose vial. The package contains 25 vials. The label includes storage information and states the product is from Fresenius Kabi USA, LLC.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Label for Heparin Sodium Injection, USP, 30,000 units per 30 mL (1,000 USP units per mL) from Fresenius Kabi USA, LLC. The label indicates it is from porcine intestinal mucosa and is for intravenous or subcutaneous use. Storage instructions specify 20°C to 25°C controlled room temperature. The label includes directions to see the insert for dosage and usage, and a barcode is visible.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Packaging label for Heparin Sodium Injection, USP with a strength of 30,000 USP units per 30 mL (1,000 USP units per mL). The label indicates it is for intravenous or subcutaneous use and comes in a package of 25 vials. The product is labeled by Fresenius Kabi USA, LLC and includes storage instructions and ingredients info.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Label for Heparin Sodium Injection, USP 50,000 USP units per 5 mL (10,000 USP units per mL) by Fresenius Kabi USA, LLC. The vial is for intravenous or subcutaneous use, multi-dose, with instructions to not flush and to store at 20 to 25°C (68 to 77°F) controlled room temperature. The label also includes a barcode and a lot/expiration date section.*

FDA Label Image

Package Label (PRINCIPAL DISPLAY PANEL)

Label for Heparin Sodium Injection, USP with a strength of 50,000 USP units per 5 mL vial (10,000 USP units per mL). The label indicates a package of 25 vials and states it is for intravenous or subcutaneous use. The label includes handling instructions, storage conditions, and is marked by Fresenius Kabi USA, LLC. The label also features a barcode, NDC 63323-542-14.*

* 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.