Heparin Sodium Injection
Product Images NDC 87188-102

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 87188-102). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Plano Pharmaceuticals Inc., 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

1 (1)

Label for Heparin Sodium Injection USP 5,000 USP Units/mL, 1 mL multiple dose vial for intravenous or subcutaneous use. The label highlights storage instructions and states 'Not for lock flush.' Manufactured for Plano Pharmaceuticals Inc., Arlington Heights, IL. Includes bar code and space for lot and expiration dates.*

FDA Label Image

2 (2)

Heparin Sodium Injection, USP 5,000 USP Units/mL carton label for 1 mL multiple-dose vials. Manufactured for Plano Pharmaceuticals Inc. The label states the product is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, and is not for lock flush. The NDC is 87188-102-90. The label includes storage instructions and ingredients, and features the Plano Pharmaceuticals logo.*

FDA Label Image

Heparin Sodium Chemical Structure (Image 01)

Chemical structure diagram displaying five different molecular components labeled 1 through 5, each representing distinct sugar-based chemical moieties likely part of the heparin sodium active ingredient.*

* 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.