Heparin Sodium Injection, Solution
Product Images NDC 63323-262

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 20 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 63323-262). 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)

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Fresenius Kabi Logo (Hep0l 0005 02)

FDA Label Image

504001 (Hep0l 0005 03)

504001 (Hep0l 0005 03)
This is a description for a Heparin Sodium Injection, USP with a strength of 1,000 USP units per mL. The medication is meant for intravenous or subcutaneous use and is not intended for lock flush. The active ingredient is obtained from Porcine Intestinal Mucosa. The medication comes in a multiple dose vial and is made by Fresenius Kabi. There is no information given about the lot and expiration date.*
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504001 (Hep0l 0005 04)

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926201 (Hep0l 0005 05)

926201 (Hep0l 0005 05)
This is a description of a medication called Heparin Sodium Injection. It is a multiple dose vial containing 5000 USP units per mL of the medication. It is intended for use via the intravenous or subcutaneous routes and not for lock flush. The medication is obtained from Porcine Intestinal Mucosa and is only available via prescription from Fresenius Kabi.*
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926201 (Hep0l 0005 06)

926201 (Hep0l 0005 06)
This is a label of a heparin injection solution which contains 5,000 units of heparin in 1 mL of liquid. It is intended for intravenous or subcutaneous use and has a National Drug Code of 63323-262-06. There is also a batch number mentioned on the label.*
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504201 (Hep0l 0005 07)

504201 (Hep0l 0005 07)
This is a description of a medication with the NDC code 63323-542-09, identified as "Sodium Injection, USP" with a strength of 10,000 USP units per mL. It can be used either intravenously or subcutaneously, but cannot be used for lock flush purposes. It is sourced from porcine intestinal mucosa and is supplied in a multiple dose vial by Fresenius Kabi. The lot number is 403578 and the expiration date is not available. This medication is only available with a prescription.*
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504201 (Hep0l 0005 08)

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504509 (Hep0l 0005 09)

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504509 (Hep0l 0005 10)

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915501 (Hep0l 0005 11)

915501 (Hep0l 0005 11)
This is a description for a Sodium Injection solution for intravenous or subcutaneous use. The solution is available in a multiple-dose vial and contains 20000 USP units per ml. The solution should not be used for lock flush, and it is sourced from porcine intestinal mucosa. The manufacturer is Fresenius Kabi, and the lot and expiration date are provided on the package.*
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915501 (Hep0l 0005 12)

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504302 (Hep0l 0005 13)

504302 (Hep0l 0005 13)
The text describes a medication called "Heparin Z" which is a Sodium Injection, USP. It comes in a 3 2 M size with 5000 units per mL and can be used for both IV and SC use. It is preservative-free and the cost is $50.5m £.*
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504302 (Hep0l 0005 14)

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Package Label (PRINCIPAL DISPLAY PANEL)

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Package Label (PRINCIPAL DISPLAY PANEL)

Package Label (PRINCIPAL DISPLAY PANEL)
This is a not-available description as the text includes non-English characters and random characters.*
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Package Label (PRINCIPAL DISPLAY PANEL)

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Package Label (PRINCIPAL DISPLAY PANEL)

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Package Label (PRINCIPAL DISPLAY PANEL)

Package Label (PRINCIPAL DISPLAY PANEL)
This is a label of Sodium Injection, USP that contains 10,000 USP units per subcutaneous use.*
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Package Label (PRINCIPAL DISPLAY PANEL)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.