Heparin Sodium Injection, Solution
Product Images NDC 81952-115

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 13 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 81952-115). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hepalink Usa 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

Heparin-fig1 (Heparin Fig1)

Heparin-fig1 (Heparin Fig1)
Heparin Sodium Injection, USP 5,000 USP Units/mL in a 1 mL multiple dose vial. Label highlights that it is for intravenous or subcutaneous use and not for lock flush. The product is derived from porcine intestinal mucosa, sterile and nonpyrogenic, manufactured for Hepalink USA Inc. in China. Storage instructions specify 20° to 25°C (68° to 77°F).*
FDA Label Image

Heparin Fig10

Heparin Fig10
Heparin Sodium USP 10,000 Units/mL injection, solution label for 1 mL multiple dose vials by Hepalink USA Inc. The packaging indicates it is for intravenous or subcutaneous use, not for lock flush, and derived from porcine intestinal mucosa. The distribution origin is China and the label includes storage instructions and a barcode.*
FDA Label Image

Heparin Fig11

Heparin Fig11
Label for Heparin Sodium Injection USP, 20,000 USP Units/mL, multiple dose vial with 1 mL volume. The label states it is for intravenous or subcutaneous use, not for lock flush. It is derived from porcine intestinal mucosa, sterile, nonpyrogenic, and manufactured in China for Hepalink USA Inc. Storage instructions specify 20° to 25°C (68° to 77°F).*
FDA Label Image

Heparin Fig12

Heparin Fig12
Packaging label for Heparin Sodium Injection, USP 20,000 Units/mL by Techdow, a Hepalink Company. The label indicates a 1 mL multiple dose vial for intravenous or subcutaneous use, derived from porcine intestinal mucosa. The label includes storage instructions, ingredient information, and distributor Hepalink USA Inc., with a country of origin as China. The design features magenta and black color blocks with prominent warnings that the vial is not for lock flush.*
FDA Label Image

Heparin-fig2 (Heparin Fig2)

Heparin-fig2 (Heparin Fig2)
Packaging label for Heparin Sodium Injection USP, 5,000 Units/mL, in 1 mL multiple dose vials. The label shows the drug is for intravenous or subcutaneous use and is not for lock flush. It is distributed by Hepalink USA Inc. and derived from porcine intestinal mucosa. The label features orange, black, and white colors and includes usage and storage instructions.*
FDA Label Image

Heparin Fig3

Heparin Fig3
Label for Heparin Sodium Injection, USP 2,000 USP Units per 2 mL (1,000 USP Units per mL) single dose vial by Hepalink USA Inc. The label states it is preservative free, not for lock flush, for intravenous or subcutaneous use, and derived from porcine intestinal mucosa. It includes storage instructions (20 to 25°C), manufacturing origin (China), lot and expiration fields, and barcode.*
FDA Label Image

Heparin Fig4

Heparin Fig4
Heparin Sodium 2,000 USP Units/2 mL (1,000 USP Units/mL) Injection, USP in single dose vials. The label indicates it is preservative-free and for intravenous or subcutaneous use. Distributed by Hepalink USA Inc., this product is derived from porcine intestinal mucosa. The packaging includes storage instructions and a warning that the container closure is not made from natural rubber latex.*
FDA Label Image

Heparin Fig5

Heparin Fig5
Label for Heparin Sodium Injection, USP 1,000 USP Units/mL in a 1 mL multiple dose vial. The label highlights that it is not for lock flush and is intended for intravenous or subcutaneous use. It specifies storage conditions, states the product is sterile and nonpyrogenic, derived from porcine intestinal mucosa, manufactured in China, and labeled by Hepalink USA Inc.*
FDA Label Image

Heparin Fig6

Heparin Fig6
Heparin Sodium 1,000 USP Units/mL injection, solution for intravenous or subcutaneous use, supplied in 1 mL multiple dose vials. The label includes the Hepalink USA Inc. distributor information and a warning note stating NOT FOR LOCK FLUSH. The product is presented in a box labeled with strength, dosage form, and manufacturer details, with a yellow, white, black, and red color scheme.*
FDA Label Image

Heparin Fig7

Heparin Fig7
Label for Heparin Sodium Injection, USP, 10,000 USP Units/10 mL (1,000 USP Units/mL) multi-dose vial by Hepalink USA Inc. The label states it is for intravenous or subcutaneous use and includes storage instructions. It also warns: Not for lock flush.*
FDA Label Image

Heparin Fig8

Heparin Fig8
Heparin Sodium 10,000 USP Units per 10 mL injection solution label for intravenous or subcutaneous use, distributed by Hepalink USA Inc. The label indicates the product is derived from porcine intestinal mucosa and comes in 25 multiple dose vials. The label includes warnings such as 'Not for Lock Flush' and detailed storage and usage instructions.*
FDA Label Image

Heparin Fig9

Heparin Fig9
Label for Heparin Sodium Injection, USP 10,000 USP units/mL in a 1 mL multiple dose vial. The injection is for intravenous or subcutaneous use. It is derived from porcine intestinal mucosa, sterile, nonpyrogenic, and manufactured in China for Hepalink USA Inc. Storage temperature is 20 to 25°C (68 to 77°F). The label includes lot and expiration date fields.*
FDA Label Image

Heparin Chemical Structure (Heparin Str)

Heparin Chemical Structure (Heparin Str)
Chemical structure diagram showing various sugar and sulfate groups, representing the active ingredient Heparin Sodium. The diagram includes multiple hexose sugar rings with attached groups such as -OSO3-, -OH, and carboxylate groups, illustrating the molecular components of Heparin Sodium.*

* 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.