Heparin Sodium Injection, Solution
Product Images NDC 0781-3550

Product Visual Gallery

This gallery contains 19 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0781-3550). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sandoz 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 Chemical Structure (Heparin Str)

Chemical structure diagram of Heparin Sodium showing the molecular components and functional groups in a series of five connected sugar residues representing its polysaccharide structure.*

FDA Label Image

Heparin-fig1 (Heparin Fig1)

Label for Heparin Sodium Injection, USP, 5,000 USP Units/mL, 1 mL multiple-dose vial. The label indicates it is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, sterile and nonpyrogenic. Distributed by Sandoz Inc., Princeton, NJ, with storage instructions at 20 to 25°C. Features NDC 0781-3545-10.*

FDA Label Image

Heparin-fig2 (Heparin Fig2)

Packaging label for Heparin Sodium Injection, USP 5,000 USP Units/mL, a 1 mL multiple-dose vial solution for intravenous or subcutaneous use. The label includes manufacturer information for Shenzhen Techdow Pharmaceutical Co., Ltd., and distributor Sandoz Inc. The label displays warnings such as 'NOT FOR LOCK FLUSH' and details about storage and composition.*

FDA Label Image

Heparin-fig3 (Heparin Fig3)

Heparin Sodium Injection, USP 2,000 USP Units per 2 mL (1,000 USP Units per mL) sterile solution vial. Labeled for intravenous or subcutaneous use, preservative-free, single-dose vial. Distributed by Sandoz Inc., Princeton, NJ. Storage instructions and lot/expiration date fields shown.*

FDA Label Image

Heparin-fig4 (Heparin Fig4)

Heparin Sodium Injection, USP 2,000 USP Units/2 mL (1,000 USP Units/mL) carton label for intravenous or subcutaneous use. It is a preservative-free solution supplied in single-dose vials, derived from porcine intestinal mucosa. The label states it is made by Shenzhen Techdow Pharmaceutical and distributed by Sandoz Inc. Includes a barcode and instructions that it is for prescription use only.*

FDA Label Image

Heparin-fig5 (Heparin Fig5)

Label of Heparin Sodium Injection, USP, 1,000 USP Units/mL from Sandoz Inc. The 1 mL multiple-dose vial label states it is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, sterile, and nonpyrogenic. Storage instructions specify 20° to 25°C (68° to 77°F). The label includes NDC 0781-3538-10, barcodes, and spaces for lot number and expiration date.*

FDA Label Image

Heparin-fig6 (Heparin Fig6)

Heparin Sodium Injection, USP 1,000 USP Units/mL carton label for 1 mL multiple-dose vials. The label states use for intravenous or subcutaneous injection and indicates the product is derived from porcine intestinal mucosa. Manufactured by Shenzhen Techdow Pharmaceutical Co., Ltd. and distributed by Sandoz Inc. Includes regulatory information, barcode, and storage instructions. Label warns 'NOT FOR LOCK FLUSH.'*

FDA Label Image

Heparin-fig7 (Heparin Fig7)

Heparin Sodium Injection, USP 1000 USP Units/mL (10,000 USP Units/10 mL) multiple-dose vial label. The injectable solution is for intravenous or subcutaneous use. The label states storage temperature 20° to 25°C (68° to 77°F) and notes the product is derived from porcine intestinal mucosa. Distributed by Sandoz Inc., Princeton, NJ.*

FDA Label Image

Heparin-fig8 (Heparin Fig8)

Packaging label for Heparin Sodium Injection, USP 10,000 USP Units per 10 mL (1,000 USP Units/mL) by Sandoz Inc. The label indicates the drug is for intravenous or subcutaneous use, available in multiple-dose vials with 25 vials per package. It prominently displays 'NOT FOR LOCK FLUSH' and includes manufacturing and distribution details, with a barcode and storage instructions.*

FDA Label Image

Heparin-fig9 (Heparin Fig9)

Heparin Sodium Injection, USP, 10,000 USP Units/mL, 1 mL multiple-dose vial from Sandoz Inc. The label indicates it is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, sterile and nonpyrogenic. Storage instructions specify 20° to 25°C (68° to 77°F). The label also includes barcodes and space for lot and expiration date.*

FDA Label Image

Heparin-fig10 (Heparin Fig10)

Heparin Sodium 10,000 USP Units/mL injection, solution for intravenous or subcutaneous use. The label indicates a 25 multiple-dose vial derived from porcine intestinal mucosa, with a volume of 1 mL. It features warnings such as "NOT FOR LOCK FLUSH" and mentions that it is Rx Only. Manufactured by Shenzhen Techdow Pharmaceutical Co. and distributed by Sandoz Inc., Princeton, NJ.*

FDA Label Image

Heparin-fig11 (Heparin Fig11)

Label for Heparin Sodium Injection, USP, 20,000 USP Units/mL in a 1 mL multiple-dose vial. It is indicated for intravenous or subcutaneous use. The label includes storage instructions between 20° to 25°C, notes that the vial is sterile and nonpyrogenic, and states it is derived from porcine intestinal mucosa. Distributed by Sandoz Inc., Princeton, NJ. The label also warns 'NOT FOR LOCK FLUSH.'*

FDA Label Image

Heparin-fig12 (Heparin Fig12)

Heparin Sodium Injection, USP 20,000 USP Units/mL label for multiple-dose vials, 1 mL volume. The sterile solution is for intravenous or subcutaneous use, derived from porcine intestinal mucosa. Labeler is Sandoz Inc., distributed by Sandoz Inc. in Princeton, NJ, with manufacturing by Shenzhen Techdow Pharmaceutical Co., Ltd., China. The packaging includes a red warning stating "NOT FOR LOCK FLUSH."*

FDA Label Image

Heparin-fig13 (Heparin Fig13)

Heparin Sodium Injection, USP label showing 1,000 USP Units/mL strength, 30 mL multiple-dose vial for intravenous or subcutaneous use. The label states 30,000 USP Units per 30 mL vial, derived from porcine intestinal mucosa, sterile and nonpyrogenic. Distributed by Sandoz Inc., Princeton, NJ. Storage instructions and barcode also visible.*

FDA Label Image

Heparin-fig14 (Heparin Fig14)

Heparin Sodium Injection, USP solution carton label for 30,000 USP units/30 mL (1,000 USP units/mL) multiple-dose vials. For intravenous or subcutaneous use, derived from porcine intestinal mucosa. Distributed by Sandoz Inc., manufactured by Shenzhen Techdow Pharmaceutical Co., Ltd. The label includes storage instructions and formulation details. "Not for lock flush" is prominently noted.*

FDA Label Image

Heparin-fig15 (Heparin Fig15)

Heparin Sodium Injection, USP label for a 5 mL multiple-dose vial, strength 50,000 USP Units/5 mL (10,000 USP Units/mL). The label notes use for intravenous or subcutaneous administration. It includes storage instructions at 20° to 25°C, indicates it is derived from porcine intestinal mucosa, and lists Sandoz Inc. as the distributor located in Princeton, NJ.*

FDA Label Image

Heparin-fig16 (Heparin Fig16)

Heparin Sodium Injection, USP 50,000 USP Units/5 mL (10,000 USP Units/mL) solution for intravenous or subcutaneous use, in a 5 mL multi-dose vial. The label indicates it is Rx only, derived from porcine intestinal mucosa, and distributed by Sandoz Inc. The packaging includes the note 'NOT FOR LOCK FLUSH' and storage instructions.*

FDA Label Image

Heparin-fig17 (Heparin Fig17)

Heparin Sodium Injection, USP label for a 10 mL multiple-dose vial with a strength of 50,000 USP Units per 10 mL (5,000 USP Units/mL). The label indicates intravenous or subcutaneous use and contains a warning about benzyl alcohol. Distributed by Sandoz Inc., Princeton, NJ. Storage instructions specify 20° to 25°C (68° to 77°F).*

FDA Label Image

Heparin-fig18 (Heparin Fig18)

Packaging label for Heparin Sodium Injection, USP by Sandoz Inc. The label specifies a strength of 50,000 USP Units/10 mL (5,000 USP Units/mL). It includes warnings about containing benzyl alcohol, intended for intravenous or subcutaneous use in multiple-dose vials. The label also features the product NDC 0781-3550-25, manufacturer information listing Shenzhen Techdow Pharmaceutical Co., Ltd. as the manufacturer and Sandoz Inc. as the distributor, and a barcode. The label prominently displays "NOT FOR LOCK FLUSH" and dosing instructions.*

* 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.