Heparin Sodium Injection, Solution
Product Images NDC 0409-2720

This is a description of a pharmaceutical product contained in a 1mL single-dose vial with Rx-only prescription. The product belongs to the HEPARI category for subcutaneous use and is derived from Porcine Bz. It contains 1,000 usp unity per mL and should not be used for lock flush. There are several non-readable characters throughout the text.*

This is a description of a 10 mL multi-dose vial containing Heparin, which is obtained from Porcine intestines. It is used for intravenous or subcutaneous use with a dosage specified in the insert. Each mL of the vial contains 1000 USP units of heparin sodium, sodium chloride, benzyl alcohol, and water or injection. The pH of the solution is adjusted using NaOH and Hel if necessary. The vial is prescribed under RX Only and has an NDC code of 0409-2720-31. The usual storage temperature is between 20 to 25 degrees Celsius. It is distributed by Hospira, Inc. with a LOT number and EXP date provided.*

This is a description for a 30 mL multi-dose vial with the NDC number 0409-2720-32. Each mL of the vial contains 8.6 mg of heparin sodium and 0.01 mL of benzyl alcohol in injectable water for injection with pH range of 5.0-7.5. Sodium Injection, USP and/or HCL can be added, if necessary, to adjust pH. The usual dosage is mentioned in the insert. The vial has 30,000 USP Units per 30 mL. It is meant for intravenous or subcutaneous use and should be stored at 20 to 25°C (68 to 77°F). It can be stored at controlled room temperature under USP guidelines. The manufacturer is Hospira, Inc, and the product is derived from Porcine Intestines. Lot # and expiration date are also mentioned.*

This is a description of an injectable solution of heparin sodium. It is non-pyrogenic and should be stored at room temperature. The package inset should be consulted for dosage instructions. The solution contains heparin sodium, alcohol, water for injection, sodium chloride, and benzyldium hydroxide and/or hydrochloric acid for pH balance. The origin of manufacture is Spain, and the distributor is Hosp.*

This appears to be a label for a sodium injection of Heparin. The concentration is 10,000 units/mL, and it is not recommended for lock flush use. There are also instructions to tear the label at a certain point. The remaining text appears to be random characters and symbols.*

This is a product label from a 1mL single-dose vial containing 5,000 USP units/mL of a solution sourced from porcine intestines and containing a preservative. The label includes directions to tear at a marked spot and a warning that the product is not for lock flush. The label provides a lot number and expiration date.*

This is a description of a 10 mL Multi-dose Vial of Heparin Sodium Injection, USP obtained from porcine intestines. It contains 50,000 USP Units/10mL and is used for Intravenous or Subcutaneous administration. The usual dosage should be seen in the insert. The vial should be stored at 20-25°C (68-77°F) and is for Rx use only. It is distributed by Hospira, Inc, Lake Forest IL60045 USA. There are specific LOT and EXP details on this product.*

This is a HEPARIN sodium injection solution, USP, for intravenous or subcutaneous use. It contains 50,000 USP units/10mL and comes in a 10mL multi-dose vial (NDC 0409-2723-02). It is derived from porcine intestines and has a concentration of 1000 USP units/mL. The lot number is not available.*