Heparin Sodium
Product Images NDC 0641-2450

Product Visual Gallery

This gallery contains 18 technical images submitted to the FDA as part of the official labeling for Heparin Sodium (NDC 0641-2450). 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.

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Chemical Structure (Heparin Sodium Injection Usp 1)

This appears to be a set of instructions or labels for a product. The first line contains the command "R" with some symbols and characters that are not clear, followed by the instruction "Remove" and the text "a0 b". The second line seems to indicate that there is an "External Collar" present, but that it should not be removed.*

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

This is a description of a drug labeled NDC 0641-2460-30 R, which contains heparin sodium and sodium chloride. It is stored at room temperature and can be administered intravenously or subcutaneously. The drug is available in a 10 mL multiple dose vial. The text also mentions that NaDH and HE! can be added if needed.*

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

This is a description of a medication called o3, which is available in a package of 25 x 10 mL Multi Dose Vials. Each mL of this medication contains 5,000 USP units of sodium heparin, 7mg of sodium chloride and 0.01 mL of benzyl alcohol in water for injection. The medication is used for Intravenous or Subcutaneous Use and is made by Hikma Pharmaceutical. The dosage is described in the package insert and the medication should be stored at 20°-25°C (68°-77°F).*

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Heparin Sodium Injection Usp 12

This is a description of Heparin Sodium Injection, USP which comes in a 30 mL Multiple Dose Vial with 30,000 use units/30 mL concentration. The injection is for intravenous or subcutaneous usage and contains heparin sodium, sodium chloride, and benzyl lconol in water for injection. The pH of the injection is adjusted with NaOH and/or HCI. The injection should be stored between 20°C-25°C and is manufactured by Hikma in Eatontown, NJ.*

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Heparin Sodium Injection Usp 13

This is a description of a medication called NDC 0641-2450-55 R. It is not suggested for use on Lock Flush. The medication is made from Porcine Intestines, and every mL of the drug contains heparin sodium, sodium chloride 8.6 mg, and benzyl alcohol 0.01 mL in Water for Injection. The pH of the solution ranges from 5.0 to 7.5, and NaOH and/or HCI added, if needed, for pH adjustment. The usual dosage is available through package insert. The medication is sold in a multiple dose vial of 25 x 30 mL, and each vial contains 30,000 use units/30 mL. The medication should be stored at 20°-25°C (68°-77°F). The drug is made by Hikma, Eatontown, NJ 07724 USA, and it is suggested for Intravenous or Subcutaneous Use only.*

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Heparin Sodium Injection Usp 14

This appears to be the label or packaging information for a 0.5mL single dose syringe manufactured by the company Hikma. The syringe contains EEMREISRIEY USP units/0.5mL and is recommended for intravenous (IV) or subcutaneous (SC) use. It is also noted that the syringe is preservative-free. The packaging includes a product code, NDG 0641-6204-01 462-855-00.*

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Heparin Sodium Injection Usp 15

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Heparin Sodium Injection Usp 16

This appears to be the description of a 1L Single Dose Syringe by Hikma that contains 05mL to 1ml of ARSI USP uniits/m. The syringe is intended for use via IV or SC and is free of preservatives. The NDC number is 0641-6199-01 and it has a lot number of Fd. There is an expiration date provided but it is not visible in the text.*

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Heparin Sodium Injection Usp 17

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Heparin Sodium Injection Usp 18

This text contains product information such as the GTIN (Global Trade Item Number), SN (Serial Number), EXP (Expiration Date), and LOT (Lot Number). It appears to be a sample or example format and does not provide any specific information about a particular product.*

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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)

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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)

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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)

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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)

This is a description of a heparin injection that is derived from porcine intestines. It contains 1,000 USP units of heparin sodium along with sodium chloride and benzyl alcohol in water for injection. The pH level is between 5.0-7.5, adjusted using NaOH or HCI. It is intended for intravenous or subcutaneous use and comes in 25% 1mL vials manufactured by Hikma in Eatontown, NJ.*

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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)

This is a label for a medication produced by the company Hikma. The medication can be administered either intravenously (IV) or subcutaneously (SC). Any other important information about the medication, such as dosage or indications, is not available in the provided text.*

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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)

This is a product description of Sodium Injection, USP which is used for Intravenous or Subcutaneous Use. Each vial contains 5,000 USP units/mL of heparin sodium, sodium chloride, and benzyl alcohol in Water for Injection. The pH can be adjusted using NaOH and/or HCI. The usual dosage is mentioned in the package insert. The product should be stored at controlled room temperature. The manufacturer is Hikma located in Eatontonn, NJ, USA.*

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

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

This text describes an injectable solution containing heparin derived from porcine intestines, with each L containing 10,000 USP units of heparin sodium, sodium chloride, and benzylalconol in water. The solution can be used for pH adjustment and is recommended to be stored at a controlled room temperature. It is manufactured by Hikma in Eatontown, NJ.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.