Heparin Sodium Injection
Product Images NDC 0641-6199

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0641-6199). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals 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

Chemical Structure (Heparin Sodium Injection Usp 1)

An instructional diagram of a 1 mL single dose syringe for Heparin Sodium by Hikma Pharmaceuticals USA Inc., showing labeled parts including the syringe tip cap (remove), external collar (do not remove), label, and plunger rod. A volume scale indicates 0.5 mL and 1 mL marks on the barrel.*

FDA Label Image

462-522-05 (Heparin Sodium Injection Usp 10)

Label for Heparin Sodium Injection, USP, 50,000 USP Units per 10 mL (5,000 USP Units/mL) in a 10 mL multiple dose vial. The label states it is for intravenous or subcutaneous use and specifies it is not for lock flush. Manufactured by Hikma Pharmaceuticals USA Inc., the product is derived from porcine intestines and contains sodium chloride, benzyl alcohol, and water for injection. Storage conditions and pH adjustment information are also noted.*

FDA Label Image

462-523-04 Resized (Heparin Sodium Injection Usp 11)

Label for Heparin Sodium Injection, USP, 50,000 USP Units per 10 mL (5,000 USP Units/mL) multiple dose vials, 25 x 10 mL. Indicated for intravenous or subcutaneous use. Manufactured by Hikma Pharmaceuticals USA Inc. The label states it is not for lock flush and provides concentration details and storage temperature instructions.*

FDA Label Image

Heparin Sodium Injection Usp 12

Heparin Sodium Injection, USP 30,000 USP Units/30 mL (1,000 USP Units/mL) multiple dose vial label. The label states it is for intravenous or subcutaneous use and emphasizes that it is not for lock flush. It includes manufacturer information: Hikma Pharmaceuticals USA Inc., Eatontown, NJ, and storage instructions at 20°-25°C (68°-77°F). The label also notes the source as porcine intestines and lists inactive ingredients sodium chloride and benzyl alcohol.*

FDA Label Image

Heparin Sodium Injection Usp 13

Label for Heparin Sodium Injection, USP 30,000 USP Units/30 mL (1,000 USP Units/mL) by Hikma Pharmaceuticals USA Inc. It indicates use for intravenous or subcutaneous administration, with 25 vials of 30 mL multiple dose vials. Includes storage instructions and details that heparin is derived from porcine intestines.*

FDA Label Image

Heparin Sodium Injection Usp 14

Heparin Sodium 5000 USP units/0.5 mL single-dose syringe label from Hikma Pharmaceuticals USA Inc. The label indicates the product is for intravenous or subcutaneous use, preservative-free, and not for lock flush. Includes a barcode, NDC 0641-6204-01, and placeholders for lot number and expiration date.*

FDA Label Image

Heparin Sodium Injection Usp 15

Packaging label for Heparin Sodium Injection USP, 5000 USP units/0.5 mL, in prefilled single dose syringes. The label specifies it is for intravenous or subcutaneous use, preservative-free, and intended for parenteral administration. Manufactured by Hikma Pharmaceuticals USA Inc., the label includes dosing instructions and storage conditions.*

FDA Label Image

Heparin Sodium Injection Usp 16

Label for Heparin Sodium Injection, USP 5000 USP units/mL in a 1 mL single-dose syringe by Hikma Pharmaceuticals USA Inc. The label indicates it is not for lock flush, preservative-free, for IV or SC use, and includes NDC and barcode details.*

FDA Label Image

Heparin Sodium Injection Usp 17

Packaging label for Heparin Sodium Injection, USP 5,000 USP units/mL by Hikma Pharmaceuticals USA Inc. The label indicates single-dose prefilled syringes, specifying intravenous or subcutaneous use, preservative-free, and for use from porcine intestines. The label includes storage instructions, usage warnings, and barcode details.*

FDA Label Image

Heparin Sodium Injection Usp 18

A product label for Heparin Sodium by Hikma Pharmaceuticals USA Inc. displaying a GTIN barcode with GTIN number, serial number (SN), expiration date (EXP), and lot number (LOT) in a small rectangular printed area. No strength or dosage form is visible on the label section shown.*

FDA Label Image

Not For Lock Flush Rx Only 1 mL Vial Ndc 0641-0391-37 Heparin Sodium Inj., Usp 1,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 2)

An instructional illustration showing two hands connecting a syringe and a vial or container, with a curved arrow indicating the action of twisting or turning one component to attach it to the other.*

FDA Label Image

Rx Only Ndc 0641-0391-12 Heparin Sodium Injection, Usp 1,000 Usp Units/ml 25 X 1 mL Vials For Intravenous Or Subcutaneous Use From Porcine Intestines Each mL Contains Heparin Sodium 1,000 Usp Units, Sodium Chloride 8.6 mg And Benzyl Alcohol 0.01 mL In Water For Injection. Ph 5.0-7.5; Naoh And/or Hci Added, If Needed, For Ph Adjustment. Usual Dosage: See Package Insert. Store At 20º-25ºc (58º-77ºf) [see Usp Controlled Room Temperature]. (Heparin Sodium Injection Usp 3)

Chemical structure diagram of Heparin Sodium showing five labeled sugar residues with their hydroxyl, carboxyl, sulfate, N-acetyl, and other substituent groups. The diagram depicts the molecular composition and connectivity characteristic of Heparin Sodium.*

FDA Label Image

Not For Lock Flush Rx Only 1 mL Vial Ndc 0641-0400-37 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 1000 USP units per mL, from Hikma Pharmaceuticals USA Inc. The label includes the product name with strength, indicates the source as porcine intestines, and specifies use for intravenous or subcutaneous injection. It shows the NDC number 0641-0391-37 and contains warnings "NOT for Lock Flush" on red backgrounds, with a tear here instruction at the lower right corner.*

FDA Label Image

Rx Only Ndc 0641-0400-12 Heparin Sodium Injection, Usp 5,000 Usp Units/ml 25 X 1 mL Vials For Intravenous Or Subcutaneous Use From Porcine Intestines Each mL Contains Heparin Sodium 5,000 Usp Units, Sodium Chloride 7 mg And Benzyl Alcohol 0.01 mL In Water For Injection. Ph 5.0-7.5; Naoh And/or Hci Added, If Needed, For Ph Adjustment. Usual Dosage: See Package Insert. Store At 20º-25ºc (58º-77ºf) [see Usp Controlled Room Temperature]. (Heparin Sodium Injection Usp 5)

Heparin Sodium Injection, USP 1,000 USP units/mL vial label by Hikma Pharmaceuticals USA Inc. The label indicates it is for intravenous or subcutaneous use and comes in a pack of 25 vials of 1 mL each. It includes information about the source (porcine intestines), inactive ingredients, and storage conditions.*

FDA Label Image

Not For Lock Flush Rx Only 1 mL Vial Ndc 0641-0410-37 Heparin Sodium Inj., Usp 10,000 Usp Units/ml From Porcine Intestines For Iv Or Sc Use (Heparin Sodium Injection Usp 6)

Heparin Sodium Injection USP 5,000 USP units/mL vial label by Hikma Pharmaceuticals USA Inc. The label states the product is sourced from porcine intestines and intended for intravenous or subcutaneous use. The label includes instructions that the vial is not for lock flush, with three repeated alerts. Barcode, lot number, and expiration date fields are visible but not filled in.*

FDA Label Image

Rx Only Ndc 0641-0410-12 Heparin Sodium Injection, Usp 10,000 Usp Units/ml 25 X 1 mL Vials For Intravenous Or Subcutaneous Use From Porcine Intestines Each mL Contains Heparin Sodium 10,000 Usp Units, Sodium Chloride 5 mg And Benzyl Alcohol 0.01 mL In Water For Injection. Ph 5.0-7.5; Naoh And/or Hci Added, If Needed, For Ph Adjustment. Usual Dosage: See Package Insert. Store At 20º-25ºc (58º-77ºf) [see Usp Controlled Room Temperature]. (Heparin Sodium Injection Usp 7)

Heparin Sodium Injection, USP 5,000 USP units/mL vial label by Hikma Pharmaceuticals USA Inc. for intravenous or subcutaneous use. The label includes dosage form, strength, usage route, package size of 25 x 1 mL vials, storage instructions, and manufacturing details. NDC 0641-0400-12 is visible.*

FDA Label Image

462-520-05 (Heparin Sodium Injection Usp 8)

Heparin Sodium Injection USP 10,000 USP units/mL vial label by Hikma Pharmaceuticals USA Inc. It specifies the product is derived from porcine intestines and is for intravenous or subcutaneous use. The label includes instructions stating "NOT for Lock Flush" and indicates the vial size as 1 mL. Barcode, lot, and expiration date fields are present.*

FDA Label Image

462-521-04 Resized (Heparin Sodium Injection Usp 9)

Heparin Sodium Injection, USP 10,000 USP units/mL vial label by Hikma Pharmaceuticals USA Inc. The label states the product is derived from porcine intestines, listing ingredients including heparin sodium, sodium chloride, benzyl alcohol, and water for injection. It indicates usage for intravenous or subcutaneous administration and storage instructions of 20°-25°C (68°-77°F). The package contains 25 vials of 1 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.