Heparin Sodium Injection
Product Images NDC 72603-267

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 72603-267). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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 (Hep Structure)

Chemical structure diagram depicting five saccharide units of heparin sodium. Each unit is labeled (1) through (5) and includes various functional groups such as sulfate, hydroxyl, acetyl, amino, and carboxyl groups consistent with the known polysaccharide structure of heparin sodium.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Vial Label (1000 1ml Container)

Label for Heparin Sodium Injection USP, 1000 USP units per mL, 1 mL single-dose vial. The label states it is for intravenous or subcutaneous use and not for lock flush. Manufactured for Northstar Rx LLC, from porcine intestinal mucosa, with lot and expiration date fields and a barcode.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Carton (1000 1ml Carton)

Packaging label for Heparin Sodium Injection USP 1000 units per mL, manufactured by NorthStar RxLLC. The label specifies a package of 25 vials, each 1 mL single-dose for intravenous or subcutaneous use. The label features a yellow and blue design with a red caution circle stating "NOT for Lock Flush." It includes storage, contents, and manufacturing details with a barcode and NDC 72603-234-25.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per 10 mL Vial Label (10000 10ml Container)

Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) multi-dose vial label. It is indicated for intravenous or subcutaneous use. The label states the manufacturer as NorthStar Rx LLC, with manufacturing in China. Additional details include composition and storage instructions.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per 10 mL Carton (10000 10ml Carton)

Folded carton label for Heparin Sodium Injection USP, 10,000 USP units per 10 mL (1,000 USP units per mL), by NorthStar RxLLC. The label specifies the product is for intravenous or subcutaneous use and includes handling instructions such as storage and non-latex container closure. Contains multiple panels including warnings, barcode, and manufacturer details.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 30,000 Usp Units Per 30 mL Vial Label (30000 30ml Container)

Label for Heparin Sodium Injection USP, 1,000 USP units per mL, in a 30 mL multi-dose vial. The label indicates a total of 30,000 USP units per vial and specifies it is for intravenous or subcutaneous use, not for lock flush. Manufactured by NorthStar Rx LLC with storage instructions at 20 to 25°C (68° to 77°F).*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 30,000 Usp Units Per 30 mL Carton (30000 30ml Carton)

Heparin Sodium 30,000 USP units per 30 mL injection carton label by NorthStar RxLLC. The label specifies it is sodium injection USP for intravenous or subcutaneous use from porcine intestinal mucosa in 25 x 30 mL multi-dose vials. A red circle states 'NOT for Lock Flush.' The label includes storage and manufacturer information and a barcode.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Vial Label (5000 1ml Container)

Heparin Sodium Injection, USP 5,000 USP units per mL in a 1 mL single-dose vial. Label indicates it is for intravenous or subcutaneous use and not for lock flush. Manufactured by Northstar Rx LLC, with product reference to porcine intestinal mucosa source.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Carton (5000 1ml Carton)

Heparin Sodium 5000 USP units per mL injection label for intravenous or subcutaneous use. The label specifies it is not for lock flush and contains 25 x 1 mL single-dose vials. Manufactured by Northstar Rx LLC, with details on composition, storage, and usage instructions. Includes barcode and regulatory information.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 50,000 Usp Units Per 10 mL Vial Label (50000 10ml Container)

Label for Heparin Sodium Injection USP, 50,000 USP units per 10 mL (5,000 USP units per mL) in a 10 mL multi-dose vial. It specifies that the product is not for lock flush and is for intravenous or subcutaneous use. Manufactured in China for Northstar Rx LLC, the label includes storage instructions and a barcode.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 50,000 Usp Units Per 10 mL Carton (50000 10ml Carton)

Heparin Sodium Injection 50,000 USP units per 10 mL multi-dose vial carton. The label states this product is for intravenous or subcutaneous use from porcine intestinal mucosa and not for lock flush. Each 10 mL vial contains 50,000 USP units of heparin sodium. The product is manufactured for NorthStar RxLLC with a National Drug Code 72603-214-25. Storage and usage instructions are also included.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per mL Vial Label (10000 1ml Container)

Heparin Sodium Injection, USP 10,000 USP units per mL, single-dose vial for intravenous or subcutaneous use. Label includes NDC 72603-501-01, manufactured in China for NorthStar Rx LLC. Not intended for lock flush. Lot and expiration date fields are blank on the label.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per mL Carton (10000 1ml Carton)

Heparin Sodium 10,000 USP units per mL injection carton label for intravenous or subcutaneous use. The label specifies 25 single-dose 1 mL vials, manufactured by Northstar Rx LLC. The label includes a caution that it is not for lock flush and contains details on ingredients and storage conditions.*

* 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.