Heparin Sodium
Product Images NDC 67457-383

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 67457-383). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional 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

Chemical Structure (Image 01)

Chemical structure diagram of Heparin Sodium showing its polysaccharide components with sulfate and hydroxyl groups, depicting the molecular arrangement typical of this anticoagulant.*

FDA Label Image

Carton 1000 Usp-1ml (Image 02)

Label for Heparin Sodium Injection, USP 1,000 units per mL by Mylan Institutional LLC. The label indicates use for intravenous or subcutaneous administration and specifies 25 single-dose vials of 1 mL each. It includes warnings such as 'NOT for LOCK FLUSH' and notes the product is derived from porcine intestinal mucosa. Storage and usage instructions are also present.*

FDA Label Image

Carton 1000 Usp-10 mL (Image 03)

Packaging label for Heparin Sodium Injection USP, 10,000 USP units per 10 mL (1,000 USP units per mL) multi-dose vials. The label indicates it is for intravenous or subcutaneous use and not for lock flush. The product is supplied by Mylan Institutional LLC in a pack of 25 vials of 10 mL each.*

FDA Label Image

Carton 1000 Usp-30 mL (Image 04)

Heparin Sodium Injection USP 30,000 USP units per 30 mL multi-dose vial carton from Mylan Institutional LLC. The label includes dosage unit information and instructions indicating it is for intravenous or subcutaneous use only and not for lock flush. The packaging also lists active ingredient components and storage instructions.*

FDA Label Image

Carton 5000 Usp-1 mL (Image 05)

The image shows the packaging label for Heparin Sodium Injection, USP 5,000 USP units per mL, produced by Mylan Institutional LLC. The box indicates 25 single-dose 1 mL vials for intravenous or subcutaneous use, with warnings including 'NOT for LOCK FLUSH.' The product is derived from porcine intestinal mucosa and includes Benzyl Alcohol as a preservative. The label notes storage at 20° to 25°C and manufacturing in India.*

FDA Label Image

Carton 5000 Usp-10 mL (Image 06)

Heparin Sodium Injection, USP 50,000 USP units per 10 mL (5,000 USP units per mL) multi-dose vial packaging label from Mylan Institutional LLC. The label indicates the product is for intravenous or subcutaneous use, not for lock flush. The package contains 25 x 10 mL multi-dose vials. Detailed warnings and storage instructions are included on the label.*

FDA Label Image

Carton 10000 Usp-1 mL (Image 07)

Packaging label for Heparin Sodium Injection USP 10,000 USP units per mL by Mylan Institutional LLC. The label indicates 25 single-dose 1 mL vials, for intravenous or subcutaneous use, not for lock flush. Contains warnings about benzyl alcohol and storage instructions at controlled room temperature.*

FDA Label Image

Carton 10000 Usp-4 mL (Image 08)

Heparin Sodium Injection USP 40,000 USP units per 4 mL multi-dose vials, packaged in 25 x 4 mL vials. The label highlights it is for intravenous or subcutaneous use only and not for lock flush. Manufactured by Mylan Institutional LLC, the product is derived from porcine intestinal mucosa.*

* 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.