Heparin Sodium Injection
Product Images NDC 71288-449

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 71288-449). 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

Hep0d 0005 01

Hep0d 0005 01
Chemical structure diagram depicting the molecular components of Heparin Sodium, highlighting various sugar units and sulfate groups typically associated with this anticoagulant drug.*
FDA Label Image

Hep0d 0005 02

Hep0d 0005 02
Heparin Sodium Injection, USP 1,000 USP units per mL label indicating this is a 1 mL single-dose vial by Meitheal Pharmaceuticals Inc. The label notes it is for intravenous or subcutaneous use and not for lock flush. The product is derived from porcine intestinal mucosa. The label includes NDC 71288-402-01 and manufacturer information.*
FDA Label Image

Hep0d 0005 03

Hep0d 0005 03
Heparin Sodium Injection, USP 10,000 USP units per 10 mL (1,000 USP units per mL) multi-dose vial label by Meitheal Pharmaceuticals Inc. The label indicates use for intravenous or subcutaneous administration and states it is not for lock flush. The label includes manufacturing information from Meitheal Pharmaceuticals in Chicago, IL.*
FDA Label Image

Hep0d 0005 04

Hep0d 0005 04
Label for Heparin Sodium Injection, USP 30,000 units per 30 mL (1,000 USP units per mL) multi-dose vial. The label states it is for intravenous or subcutaneous use, sourced from porcine intestinal mucosa, and is not for Lock Flush. Manufactured by Meitheal Pharmaceuticals Inc.*
FDA Label Image

Hep0d 0005 05

Hep0d 0005 05
Label for Heparin Sodium Injection, USP 5,000 USP units per mL, indicated for intravenous or subcutaneous use. The label notes it is a 1 mL single-dose vial, not for lock flush. Manufactured by Meitheal Pharmaceuticals Inc., sourced from porcine intestinal mucosa, with lot and expiration date fields and barcode displayed.*
FDA Label Image

Hep0d 0005 06

Hep0d 0005 06
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, intended for intravenous or subcutaneous use. The label includes dosing concentration, manufacturer Meitheal Pharmaceuticals Inc., and storage instructions, with a warning 'NOT for Lock Flush.'*
FDA Label Image

Hep0d 0005 07

Hep0d 0005 07
Label for Heparin Sodium Injection, USP 10,000 USP units per mL, a 1 mL single-dose vial. The injection is labeled for intravenous or subcutaneous use and is not for lock flush. Manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL. The label indicates the product is derived from porcine intestinal mucosa and includes an NDC barcode.*
FDA Label Image

Hep0d 0005 08

Hep0d 0005 08
Heparin Sodium Injection, USP 40,000 USP units per 4 mL (10,000 USP units per mL) multi-dose vial label. The label indicates it is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, and is not for lock flush. Manufactured by Meitheal Pharmaceuticals Inc.*
FDA Label Image

Hep0d 0005 09 V2

Hep0d 0005 09 V2
Packaging label for Heparin Sodium Injection, USP, 1,000 USP units per mL by Meitheal Pharmaceuticals Inc. The carton design is for 25 x 1 mL single-dose vials intended for intravenous or subcutaneous use, sourced from porcine intestinal mucosa. The label includes warnings such as 'NOT for Lock Flush,' storage instructions, and ingredients related to the injection formulation.*
FDA Label Image

Hep0d 0005 10 V2

Hep0d 0005 10 V2
Heparin Sodium Injection USP 10,000 units per 10 mL multi-dose vial carton by Meitheal Pharmaceuticals Inc. The packaging includes dosing and storage information, barcode, and indication for intravenous or subcutaneous use from porcine intestinal mucosa. The label states the product is not for lock flush and contains 25 vials of 10 mL each.*
FDA Label Image

Hep0d 0005 11 V2

Hep0d 0005 11 V2
Heparin Sodium Injection USP 30,000 USP units per 30 mL (1,000 USP units per mL) in multi-dose vials, labeled for intravenous or subcutaneous use from porcine intestinal mucosa. The packaging states it is not for lock flush. Labeler is Meitheal Pharmaceuticals Inc., with NDC 71288-402-31.*
FDA Label Image

Hep0d 0005 12 V2

Hep0d 0005 12 V2
Carton packaging label for Heparin Sodium Injection, USP 5,000 USP units per mL by Meitheal Pharmaceuticals Inc. The box contains 25 single-dose vials, intended for intravenous or subcutaneous use from porcine intestinal mucosa. The label includes storage instructions and a barcode.*
FDA Label Image

Hep0d 0005 13 V2

Hep0d 0005 13 V2
Packaging label for Heparin Sodium Injection USP, 50,000 USP units per 10 mL (5,000 USP units per mL) multiple-dose vials. The label indicates it is for intravenous or subcutaneous use and not for lock flush. The product is manufactured by Meitheal Pharmaceuticals Inc. This packaging contains 25 vials of 10 mL each, Rx only.*
FDA Label Image

Hep0d 0005 14 V2

Hep0d 0005 14 V2
Packaging label for Heparin Sodium Injection, USP 10,000 USP units per mL by Meitheal Pharmaceuticals Inc. The label indicates the product contains 25 single-dose vials of 1 mL each for intravenous or subcutaneous use, derived from porcine intestinal mucosa. The label prominently states 'NOT for Lock Flush' use.*
FDA Label Image

Hep0d 0005 15 V2

Hep0d 0005 15 V2
Packaging label for Heparin Sodium Injection USP, 40,000 USP units per 4 mL (10,000 USP units per mL), by Meitheal Pharmaceuticals Inc. The label states the product is for intravenous or subcutaneous use and is not for lock flush. The package size is 25 multi-dose vials of 4 mL each.*

* 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.