Heparin Sodium
Product Images NDC 67457-603

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 67457-603). 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)

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Carton 1000 Usp-1ml (Image 02)

HEPARIN Sodium Injection, USP is a medication that is commonly used for intravenous or subcutaneous use in clinics or hospitals. The package insert or complete information on dosage and administration should be consulted before use. The medication contains 1,000 USP units of heparin, as well as sodium chloride, benzyl alcohol, and water for injection. This medication may have been modified with sodium hydroxide and/or hydrochloric acid. The medication is manufactured by Mylan Institutional LLC in Rockford, IL, and is available in 25 x 1 mL single-dose vials. Storage must be at a temperature between 20-25°C (68-77°F) according to USP Controlled Room Temperature guidelines.*

FDA Label Image

Carton 1000 Usp-10 mL (Image 03)

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Carton 1000 Usp-30 mL (Image 04)

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Carton 5000 Usp-1 mL (Image 05)

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Carton 5000 Usp-10 mL (Image 06)

This is a description of a medication called Heparin Sodium Injection, which is available in 5,000, 10,000, and 50,000 units. It can be administered either intravenously or subcutaneously, according to the instructions of Mylan Institutional LLC. Heparin Sodium Injection also contains Benzyl Alcohol. The text includes various codes and numbers and may be used for reference by healthcare professionals.*

FDA Label Image

Carton 10000 Usp-1 mL (Image 07)

This is a description of HEPARIN Sodium Injection, USP, an injectable drug. It comes in a box containing 25 single-dose 1 mL vials. The drug is derived from the intestinal mucosa of pigs and is not recommended for use as a lock flush. Heparin sodium in 10,000 USP units, sodium chloride 8 mg, benzyl alcohol 10.4 mg, and water for injection are present in each milliliter of the drug. The drug's pH may be adjusted with sodium hydroxide or hydrochloric acid. The package insert should be consulted for information on dosage and administration. The drug should be kept at a temperature between 20°C to 25°C (66 to 77°F). The drug is manufactured in India by Mylan and distributed by Hylan Institutional LLC in the USA. The product contains Benzyl alcohol.*

FDA Label Image

Carton 10000 Usp-4 mL (Image 08)

* 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.