Heparin Sodium Injection
Product Images NDC 71288-402

Product Visual Gallery

This gallery contains 21 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 71288-402). 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

Structure Of Heparin Sodium (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

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per 10 mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per 10 mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 30,000 Usp Units Per 30 mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 30,000 Usp Units Per 30 mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 50,000 Usp Units Per 10 mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 50,000 Usp Units Per 10 mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per mL Carton (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

Principal Display Panel – Heparin Sodium Injection, Usp 40,000 Usp Units Per 4 mL Vial Label (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

Principal Display Panel – Heparin Sodium Injection, Usp 40,000 Usp Units Per 4 mL Carton (Hep0d 0005 15 V3)

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 specifies the product is for intravenous or subcutaneous use from porcine intestinal mucosa and is not for lock flush. The package contains 25 multi-dose vials of 4 mL each. Additional drug content and manufacturer information are displayed, including storage instructions and barcode.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Mdv Vial Label (Hep0d 0005 16)

Label for Heparin Sodium Injection, USP 1,000 USP units per mL, a 1 mL multi-dose vial for intravenous or subcutaneous use. The product is labeled as Rx only and not for lock flush. Manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, sourced from porcine intestinal mucosa. The label includes a barcode, lot, and expiration date fields.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Mdv Carton Label (Hep0d 0005 19)

Packaging label for Heparin Sodium Injection, USP 1,000 USP units per mL, manufactured by Meitheal Pharmaceuticals Inc. The label specifies the product is for intravenous or subcutaneous use, derived from porcine intestinal mucosa, and comes in 25 multi-dose vials of 1 mL each. The label also states the product is not for lock flush use and includes storage and composition details.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Mdv Vial Label (Hep0d 0005 17)

Label for Heparin Sodium Injection, USP 5,000 USP units per mL, a multi-dose vial for intravenous or subcutaneous use. The label states it is not for lock flush and indicates the product is from porcine intestinal mucosa. Manufactured by Meitheal Pharmaceuticals Inc., Chicago, IL. The NDC number is 71288-450-01.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 5,000 Usp Units Per mL Mdv Carton Label (Hep0d 0005 20)

Packaging label for Heparin Sodium Injection, USP 5,000 USP units per mL from Meitheal Pharmaceuticals Inc. The label indicates a multi-dose vial format with 25 x 1 mL doses. It specifies intravenous or subcutaneous use and states the product is derived from porcine intestinal mucosa. The label includes typical storage instructions and sterility information.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 10,000 Usp Units Per mL Mdv Vial Label (Hep0d 0005 18)

Label for Heparin Sodium Injection, USP 10,000 USP units per mL, a 1 mL multi-dose vial intended for intravenous or subcutaneous use. The label states it is not for lock flush and indicates the product is derived from porcine intestinal mucosa. Manufactured for Meitheal Pharmaceuticals Inc., Chicago, IL, USA.*

FDA Label Image

Principal Display Panel – Heparin Sodium Injection, Usp 1,000 Usp Units Per mL Mdv Carton Label (Hep0d 0005 21)

Heparin Sodium Injection USP 10,000 USP units per mL label from Meitheal Pharmaceuticals Inc. The label indicates it is for intravenous or subcutaneous use and warns the drug is not for lock flush. The package is for 25 multi-dose 1 mL vials. Additional information includes storage recommendations and a barcode.*

* 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.