Heparin Sodium Injection, Solution
Product Images NDC 63739-920

This is a description of a medication called Heparin Sodium Injection, USP. It comes in a multiple dose vial and is used for IV or SC administration. The medication is derived from Porcine Intestinal Mucosa and is sterile and nonpyrogenic. It should be stored at 20-25°C (68-77°F) and it was manufactured in India for McKesson Corporation dba SKY Packaging. A code is provided with manufacturing and expiry details.*

This is a description of a drug called Heparin Sodium Injection, manufactured by Aurobindo Pharma Limited and distributed by Memphis, TN 38141. It is a sterile, nonpyrogenic solution that should be used intravenously or subcutaneously. It comes in 25 multiple dose vials, and each mL contains 10,000 USP units of heparin sodium. It also contains methylparaben, propylparaben, and water for injection. This drug should be stored at 20-25°C and kept out of children's reach. The NDC number for this drug is 63739-964-25.*

This is a description of Heparin Sodium Injection, USP sold by McKesson Corporation in a multiple dose vial that is not intended for lock flush. It contains 50,0005%/5 (10,000 USP Units/mlL) of heparin derived from Porcine Intestinal Mucosa and is Sterile and Nonpyrogenic for IV or SC use. It should be stored at 20° to 25°C (68°to 77°F) and was manufactured in India. Product code is TS/DRUGS/13/2010 and registration number is RO P1416656.*

NDC 6373387527 is a product of Aurobindo Pharma Limited, intended for intravenous or subcutaneous use. It is a sterile, nonpyrogenic solution of Heparin Sodium Injection, USP, with 50,000 s ui/5m (10,000 USP Units/mL) content, derived from Porcine Intestinal Mucosa. The solution is available in a pack of 25 Multiple Dose Vials. The usual dosage and other relevant information are available on the insert. The solution must only be used if the solution is clear, and seal intact. The container closure of the solution is not made from natural rubber latex.*

This is a description of a Heparin solution derived from Porcine Intestinal Mucosa that is sterile and nonpyrogenic. It is meant to be used intravenously or subcutaneously and is available in a multiple dose vial of 1 mL. The product must be stored between 20 to 25°C (68 to 77°F) and is manufactured in India for McKesson. No information is available about the medication's indications or therapeutic uses.*

This is a description of a medication named Heparin Sodium Injection. It comes in a 25 multiple dose vial derived from Porcine Intestinal Mucosa for intravenous or subcutaneous use. Each mL of the sterile, nonpyrogenic liquid contains 20,000 units of heparin sodium, 1.5 mg of methylparaben, 0.15 mg of propylparaben, and water for injection. The usual dosage instructions can be found on an insert. The container closure is not made from natural rubber latex. Store it at a temperature range of 20° to 25°C (68° to 77°F) and out of the reach of children.*

This is a description of a sterile and non-pyrogenic Heparin Sodium Injection (1,000 USP Units/mL) derived from porcine intestinal mucosa, with preservative free and for intravenous or subcutaneous use. The product is stored in room temperature and produced in India for McKesson Corporation. The package contains a 2mL single dose vial with instructions to discard any unused portion. It is important not to use the product to lock flush.*

This is a description of Heparin Sodium Injection, USP. The product is manufactured by Aurobindo Pharma Limited in India, and distributed by McKesson Corporation in Memphis, Tennessee. It is a sterile, nonpyrogenic solution for intravenous or subcutaneous use and is derived from porcine intestinal mucosa. Each single-dose vial contains 1,000 USP units of heparin sodium, 9 mg of sodium chloride, and water for injection. Hydrochloric acid and/or sodium hydroxide may have been added for pH adjustment. This product is not intended for use as a lock flush. Usual dosage instructions are provided in the product insert. The solution should be clear and the seal intact before use. The drug should be stored at 20 to 25°C and kept out of the reach of children. The container closure is not made from natural rubber latex.*

This is a description of a medication called Heparin, which is derived from Porcine Intestinal Mucosa. It is sterile and nonpyrogenic and should be stored at a temperature range of 20-25°C (68-77°F). The medication comes in a 10 mL multiple-dose vial and can be used for IV or SC administration only. The packaging was done in India for McK and has an NDC code of 63739-901-14. The medication contains Benzyl Alcohol and should not be used for lock flush purposes. The text contains a lot of errors and minor typos.*

This is a description of a medicine called "HEPARIN NOT SODIUM INJECTION, USP FOR LOCK" that is available in a 50,000 USP Units/10 mL presentation. It is a sterile, nonpyrogenic solution suitable for intravenous or subcutaneous use. It should only be used if the solution is clear and the seal is intact. The medicine is manufactured by "intact." and distributed by McKesson Corporation dba SKY Packaging. The usual dosage is available in the insert. The container closure is not made from natural rubber latex. The medicine is derived from porcine intestinal mucosa.*

This text seems to be a description of a medication, specifically Heparin Sodium Injection, USP, which is used for intravenous or subcutaneous use. The medication is manufactured by Aurcbindo Pharma Limited and distributed by McKesson Corporation. Each milliliter contains 1,000 units heparin sodium, 9 mg sodium chloride, 1.5 mg methylparaben, and 0.15 mg propylparaben. The pH of the medication may have been adjusted with sodium hydroxide or hydrochloric acid. The medication should be stored at 20°C to 25°C (68°F to 77°F) and should only be used if the solution is clear. The usual dosage can be found in the insert.*

This is a description of a medical product called Heparin, which is derived from porcine intestinal mucosa. It is a sterile and nonpyrogenic solution that is meant to be stored at temperatures between 20-25°C. The solution is designed for intravenous or subcutaneous use and comes in a multiple-dose vial of 10mL. The package has a warning to keep the drug out of reach of children and is not to be used for lock flush. The packaging is manufactured in India for McKesson Corporation with the code TSIDRUGS/13/2010 E E. The batch was produced in July 2018.*

HEPARIN SODIUM INJECTION, USP is a medication derived from Porcine Intestinal Mucosa, manufactured by Aurobindo Pharma Limited in India and distributed by McKesson Corporation in the US. Each multiple dose vial contains 10,000 USP Units in 10mL of nonpyrogenic, sterile solution for intravenous or subcutaneous use. The solution is isotonic with sodium chloride, and sodium hydroxide and/or hydrochloric acid may have been added for pH adjustment. The package contains 25 vials and has a shelf life of two years under controlled room temperature. The usual dosage recommendation is provided in the insert, and users are advised to check that the solution is clear and seal intact before use. The product is not made from natural rubber latex and should be kept out of reach of children.*

Description: LTy R TP S R VL LTVl is a sterile, nonpyrogenic solution derived from porcine intestinal mucosa that contains heparin. It is intended for intravenous or subcutaneous use and is supplied in a multiple-dose vial of 30 mL. The product should be stored at 20° to 25°C (68° to 77°F) and kept out of reach of children. It was manufactured in India for McKesson Corporation and has a code of TSIDRUGS/13/2010.*

This is a description of the drug Heparin Sodium Injection, made by Aurobindo Pharma Limited and distributed by McKesson Corporation dba SKY Packaging. It is a sterile and nonpyrogenic solution intended for Intravenous or Subcutaneous use, derived from Porcine Intestinal Mucosa. Each mL contains 1,000 USP units of Heparin sodium, 9mg sodium chloride, and other ingredients such as methylparaben and propylparaben. The text includes information on storage, dosage, and precautions.*

This is a pharmaceutical product called "SODIM INJECTION, USP," which is derived from porcine intestinal mucosa. It is a sterile and non-pyrogenic substance that can be used for intravenous (IV) or subcutaneous (SC) purposes. The product is stored at a temperature between 20 to 25°C (68°F to 77°F) and comes in a multiple-dose vial of 1 mL. It is manufactured in India for McKesson Corporation dba SKY Packaging with a product code of "TSIDRUGS/13/2010_ .. R07/2018 __P1416661".*

This is a description of HEPARIN SODIUM INJECTION which is distributed by McKesson Corporation. It is intended for Intravenous or Subcutaneous use and comes in a 25 Multiple Dose Vials package. Each mL of HEPARIN SODIUM INJECTION contains 5,000 USP units heparin sodium, 5 mg sodium chloride, 1.5 mg methylparaben, and 0.15 mg propylparaben, and is derived from Porcine Intestinal Mucosa. The usual dosage is mentioned in the insert, and it should be used only if the solution is clear and the seal is intact. It should be stored at a temperature of 20° to 25°C (68° to 77°F) and out of the reach of children. The container closure is not made from natural rubber latex.*

This is a description of a Heparin solution derived from Porcine Intestinal Mucosa. It is a sterile and nonpyrogenic solution intended for intravenous or subcutaneous administration. The solution is stored at a temperature range of 20° to 25°C. The Heparin solution is manufactured in India for McKesson Corporation dba SKY Packaging, and it is contained in a multiple-dose vial with a volume of 1 mL.*