Heparin Sodium Injection
Product Images NDC 71288-400

3 FDA label images from Meitheal Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 71288-400). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Meitheal 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

Hep0b 0003 01

Hep0b 0003 01
Chemical structure diagram showing multiple sugar moieties, representing the molecular components of heparin sodium. The labeled structures include various sulfate, hydroxyl, acetyl, and carboxyl groups characteristic of heparin polysaccharides.*
FDA Label Image

Hep0b 0003 02

Hep0b 0003 02
Label for Heparin Sodium Injection, USP 2000 units per 2 mL single-dose vial. The preservative-free injection is for intravenous or subcutaneous use, not for lock flush. Manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, sourced from porcine intestinal mucosa, with NDC 71288-400-02.*
FDA Label Image

Hep0b 0003 03

Hep0b 0003 03
Heparin Sodium Injection, USP 2,000 USP units per 2 mL (1,000 USP units per mL) single-dose vials packaging label. The label includes warnings 'NOT for Lock Flush' and indicates the product is preservative-free for intravenous or subcutaneous use from porcine intestinal mucosa. The labeler is Meitheal Pharmaceuticals Inc., NDC 71288-400-03. The carton contains 25 x 2 mL single-dose vials with instructions to discard unused portions.*

* 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.