Heparin Sodium Injection, Solution
Product Images NDC 63323-276

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 63323-276). 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 (Hep0n 0001 01)

Chemical structure diagram of Heparin Sodium showing the detailed molecular components of the active ingredient as depicted in the image.*

FDA Label Image

Logo (Hep0n 0001 02)

FDA Label Image

504001 (Hep0n 0001 03)

Label for Heparin Sodium Injection, USP, showing strength 1,000 USP Units per mL. The label includes instructions 'Not For Lock Flush' in black text on a yellow background. The product is from Fresenius Kabi USA, LLC. The label emphasizes it is for injection and includes volume information of 1 mL.*

FDA Label Image

504001 (Hep0n 0001 04)

Heparin Sodium Injection, USP 1000 USP units per mL in 1 mL vials. The label indicates it is for intravenous or subcutaneous use, distributed by Fresenius Kabi USA, LLC. The package contains 25 vials and includes usage and storage instructions, as well as warnings such as 'Not for Lock Flush.' A barcode and NDC 63323-540-01 are also shown.*

FDA Label Image

926201 (Hep0n 0001 05)

Heparin Sodium Injection, USP label for 5,000 USP units per mL solution. The label prominently displays warnings "NOT FOR LOCK FLUSH" on bright yellow and black bands. The product is indicated for intravenous or subcutaneous administration and is manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

926201 (Hep0n 0001 06)

Heparin Sodium Injection, USP 5,000 units per mL vial label by Fresenius Kabi USA, LLC. The label indicates the product is for intravenous or subcutaneous use, contains 1 mL per vial, and comes in a package of 25 vials. The label includes storage instructions and a barcode, along with the NDC number 63323-262-01.*

FDA Label Image

504201 (Hep0n 0001 07)

Heparin Sodium Injection, USP label showing 10,000 USP units per mL strength. The dosage form is solution for intravenous or subcutaneous injection. The label features a brown and white color scheme with warnings not to flush or lock, and instructions for use. The product is labeled by Fresenius Kabi USA, LLC.*

FDA Label Image

504201 (Hep0n 0001 08)

Heparin Sodium Injection label showing 10,000 USP units per mL strength in a 1 mL vial. The label includes usage instructions for intravenous or subcutaneous injection, cautions not to lock the plunger in the vial, and indicates the product is supplied in a package of 25 vials. The manufacturer is Fresenius Kabi USA, LLC.*

FDA Label Image

504509 (Hep0n 0001 09)

Heparin Sodium Injection, USP vial label showing 40,000 USP units per 4 mL (10,000 USP units per mL) strength. The label includes administration routes intravenous or subcutaneous and a yellow vertical warning strip stating 'NOT FOR LOCK FLUSH'. The product is from Fresenius Kabi USA, LLC.*

FDA Label Image

504509 (Hep0n 0001 10)

Label for Heparin Sodium Injection, USP 40,000 units per 4 mL (10,000 USP units per mL) by Fresenius Kabi USA, LLC. The label specifies intravenous and subcutaneous use and contains warnings about the heparin content and acetyl alcohol. Package contains 25 vials.*

FDA Label Image

915501 (Hep0n 0001 11)

Packaging label for Heparin Sodium Injection, USP, with a strength of 20,000 USP units per mL. The label includes a warning section in yellow and black stating "NOT FOR LOCK FLUSH". The label also indicates that the product is for intravenous or subcutaneous use and contains 1 mL per unit dose. The labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

915501 (Hep0n 0001 12)

Heparin Sodium Injection, USP, 20,000 USP units per mL, 1 mL vial. Label includes drug name, strength, dosage form, route of administration (intravenous or subcutaneous), and directions to not lock the push. The package contains 25 vials and is labeled by Fresenius Kabi USA, LLC.*

FDA Label Image

27602 (Hep0n 0001 13)

Heparin Sodium Injection, USP label with a strength of 1,000 USP units per mL, in a 2 mL volume totaling 2,000 USP units. The label indicates it is preservative free, for intravenous or subcutaneous use, and directs that it is from porcine intestinal mucosa, single dose vial. The labeler is Fresenius Kabi USA, LLC. The top portion includes a yellow and black warning stating 'NOT FOR LOCK FLUSH'.*

FDA Label Image

27602 (Hep0n 0001 14)

Heparin Sodium Injection, USP 2,000 units per 2 mL (1,000 USP units per mL) single dose vial vial label. The label indicates 25 vials per package, preservative free, for intravenous or subcutaneous use. Made by Fresenius Kabi USA, LLC. The label includes warnings such as 'Not for lock flush' and states the drug is preservative free, nonpyrogenic, and contains no natural rubber latex.*

FDA Label Image

4710 (Hep0n 0001 15)

Heparin Sodium Injection, USP label showing a strength of 50,000 USP units per 10 mL (5,000 USP units per mL) for intravenous or subcutaneous use. The label also includes warnings about benzyl alcohol, dosing instructions, storage conditions, manufacturer Fresenius Kabi USA, LLC, and a barcode.*

FDA Label Image

4710 (Hep0n 0001 16)

Heparin Sodium Injection, USP 50,000 units per 10 mL (5,000 USP units per mL) in a multiple dose vial. Label indicates 25 vials per package for intravenous or subcutaneous use. The label includes warnings, storage instructions, and barcodes, manufactured by Fresenius Kabi USA, LLC.*

FDA Label Image

504302 (Hep0n 0001 17)

Heparin Sodium Injection, USP 5,000 units per 0.5 mL solution label. The label displays the product name, strength, and volume, with instructions indicating it is not for lock flush use. It is intended for intravenous or subcutaneous administration and includes a preservative-free designation. The labeler is Fresenius Kabi USA, LLC.*

FDA Label Image

504302 (Hep0n 0001 18)

Label for Heparin Sodium Injection, USP, 5,000 USP units per 0.5 mL, an intravenous or subcutaneous injection solution. The label notes it is preservative-free and contains 25 vials. The labeler is Fresenius Kabi USA, LLC. Additional handling and composition details are printed on the label.*

* 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.