Heparin Sodium Injection, Solution
Product Images NDC 25021-402

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 25021-402). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sagent Pharmaceticals, 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 (representative Subunits) (Hep08 0007 01)

Chemical structure diagram of Heparin Sodium showing its five key sugar moieties with functional groups indicated, representing the molecular components of this anticoagulant agent.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Hep08 0007 02)

Label for Heparin Sodium Injection, USP 1,000 USP units per mL in a 1 mL vial. The label states it is for intravenous or subcutaneous use and derived from porcine intestine. Manufactured for Sagent Pharmaceuticals by Premier ProRx, made in India. The label includes an NDC number and instructions not for lock flush use.*

FDA Label Image

Package Label – Principal Display Panel – Carton (Hep08 0007 03)

Heparin Sodium Injection, USP 1,000 USP units per mL, 1 mL vial packaging label by Sagent Pharmaceuticals. The label indicates a package size of 25 vials and includes safety warnings like 'NOT FOR LOCK FLUSH.' The label design features yellow and red colors with vial images and barcodes.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Hep08 0007 04)

Label for Heparin Sodium Injection, USP 5,000 USP units per mL in a 1 mL vial. It is a prescription drug for intravenous or subcutaneous use. The label indicates it is manufactured for Sagent Pharmaceuticals, Schaumburg, IL, and made in India. The label includes a barcode and a warning area labeled 'Un Varnish Area 18 x 8 mm.'*

FDA Label Image

Package Label – Principal Display Panel – Carton (Hep08 0007 05)

Carton label for Heparin Sodium Injection, USP 5,000 USP units per mL, 1 mL vials. The package contains 25 vials and is labeled for intravenous and subcutaneous use. The labeler is Sagent Pharmaceuticals, featuring a yellow and orange design with the vial image displayed and instructions stating 'NOT FOR LOCK FLUSH.'*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Hep08 0007 06)

Label for Heparin Sodium Injection, USP, 10,000 USP units per mL, in a 1 mL vial. The label indicates it is for intravenous or subcutaneous use and derived from porcine intestines. Manufactured for Sagent Pharmaceuticals by Premier ProRx in India. Includes a caution 'NOT FOR LOCK FLUSH' and a barcode.*

FDA Label Image

Package Label – Principal Display Panel – Carton (Hep08 0007 07)

Heparin Sodium 10,000 USP units per mL injection solution label by Sagent Pharmaceuticals. The label indicates 1 mL vial volume with 25 vials per carton. Warning 'Not for Lock Flush' is printed in yellow. The design features brown and yellow colors with dosage and manufacturer details.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Hep08 0007 08)

Heparin Sodium Injection, USP 10,000 USP units per mL in a 10 mL multi-dose vial. The label states it is not for lock flush and is intended for intravenous or subcutaneous use from porcine intestines. Manufactured by Sagent Pharmaceuticals under the Premier Pro Rx brand.*

FDA Label Image

Package Label – Principal Display Panel – Carton (Hep08 0007 09)

Packaging label for Heparin Sodium Injection, Solution, 10,000 USP units per mL strength, presented in 10 mL multi-dose vials. The label indicates a package containing 25 vials, manufactured by Sagent Pharmaceuticals under the PremierProRx brand. The label features warnings such as "NOT FOR LOCK FLUSH" and specifies intravenous or subcutaneous use.*

FDA Label Image

Package Label – Principal Display Panel – Vial Label (Hep08 0007 10)

Heparin Sodium Injection, USP 30,000 USP units per 30 mL (1,000 USP units per mL) multi-dose vial label by Sagent Pharmaceuticals. The label specifies that the product is for intravenous or subcutaneous use from porcine intestines and includes storage instructions. The NDC is 25021-400-68.*

FDA Label Image

Package Label – Principal Display Panel – Carton (Hep08 0007 11)

Heparin Sodium Injection, USP 30,000 USP units per 30 mL multi-dose vial label by Sagent Pharmaceuticals. The label shows a vial image prominently with the strength of 30,000 USP units per 30 mL and highlights the vial count of 25. The packaging includes caution text 'NOT FOR LOCK FLUSH' and indicates usage for intravenous and subcutaneous routes.*

* 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.