Product Images Heparin Sodium

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.*

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.*

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).*

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.*

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.*

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.*

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.*

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.*

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.*

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.*

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.*

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.*