Heparin Sodium Injection
Product Images NDC 72572-255

6 FDA label images from Civica, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 72572-255). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Civica, 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

Chemical Structure (Heparin Sodium Injection Usp 1)

Chemical Structure (Heparin Sodium Injection Usp 1)
Chemical structure diagram of Heparin Sodium showing its complex polysaccharide components and functional groups commonly found in the molecule.*
FDA Label Image

Rx Only 1 mL Vial Ndc 72572-250-01 Heparin Sodium Inj., Usp 1,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 2)

Rx Only 1 mL Vial Ndc 72572-250-01 Heparin Sodium Inj., Usp 1,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 2)
Label of Heparin Sodium Injection USP 1000 USP units/mL, 1 mL vial by Civica, Inc. The label specifies the drug is sourced from porcine intestines and intended for intravenous or subcutaneous use. It includes warnings 'NOT for Lock Flush' and a section for lot number and expiration date.*
FDA Label Image

Ndc 72572-250-25 Rx Only Heparin Sodium Injection, Usp 1,000 Usp Units/ml For Intravenous Or Subcutaneous Use 25 X 1 mL Vials (Heparin Sodium Injection Usp 3)

Ndc 72572-250-25 Rx Only Heparin Sodium Injection, Usp 1,000 Usp Units/ml For Intravenous Or Subcutaneous Use 25 X 1 mL Vials (Heparin Sodium Injection Usp 3)
Label for Heparin Sodium Injection, USP 1,000 USP units/mL, an intravenous and subcutaneous injection. The label shows a 25 x 1 mL vial packaging. It includes storage instructions, excipients, and manufacturer details: Civica, Inc. and Hikma Pharmaceuticals USA Inc. The NDC is 72572-250-25 and the label indicates Rx only.*
FDA Label Image

Rx Only 1 mL Vial Ndc 72572-255-01 Heparin Sodium Inj., Usp 5,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 4)

Rx Only 1 mL Vial Ndc 72572-255-01 Heparin Sodium Inj., Usp 5,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 4)
Label for Heparin Sodium Injection USP 5,000 USP units/mL in a 1 mL vial, manufactured for Civica, Inc. The label indicates the drug is sourced from porcine intestines and intended for intravenous or subcutaneous use. The label also includes usage caution 'NOT for Lock Flush' repeated three times on a red background.*
FDA Label Image

Ndc 72572-255-25 Rx Only Heparin Sodium Injection, Usp 5,000 Usp Units/ml For Intravenous Or Subcutaneous Use 25 X 1 mL Vials (Heparin Sodium Injection Usp 5)

Ndc 72572-255-25 Rx Only Heparin Sodium Injection, Usp 5,000 Usp Units/ml For Intravenous Or Subcutaneous Use 25 X 1 mL Vials (Heparin Sodium Injection Usp 5)
Label for Heparin Sodium Injection, USP 5,000 USP units/mL, sterile solution for intravenous or subcutaneous use. Pack contains 25 single-dose 1 mL vials. Manufactured for Civica, Inc., with details on composition, storage at controlled room temperature, and USP controlled room temperature conditions. NDC 72572-255-25, Rx only.*
FDA Label Image

Layout 1 (Heparin Sodium Injection Usp 6)

Layout 1 (Heparin Sodium Injection Usp 6)
Label from Heparin Sodium injection by Civica, Inc. showing a GTIN barcode, serial number, expiration date placeholder (MMYYYY), and lot number. The label does not display specific strength or volume information.*

* 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.