heparin sodium hospira

HEPARIN SODIUM INJECTION | Pfizer

This product information is intended only for residents of the United States. for Healthcare professionals: Heparin Sodium in 0.45% Sodium Chloride Injection - IV Bags U.S. Physician Prescribing Information. Heparin Sodium in 5% Dextrose Injection - IV Bags 20000/500mL and 25000/500mL U.S. Physician Prescribing Information. Heparin Sodium in 5% ...

Heparin Sodium Injection, 1000 Units, 1,000 U / mL 30mL ...

NDC Number 00409-2720-03 / 00409272003 Manufacturer: Hospira/Pfizer Application Anticougulant Strength: 1,000 U / mL (30,000 units / 30mL) Generic Heparin Sodium, Porcine, Preservative Free Multiple Dose Vial Storage Requirements USP Controlled Room Temperature Type Intramuscular, Intravenous, or Subcutaneous Volume 30 mL Sold as EACH.

HOSPIRA ANNOUNCES IMPORTANT SAFETY …

Sodium Chloride Heparin Lock Flush Solution Hospira has not received any reports of adverse events related to this issue to date. The company has identified the root cause to be due to a manufacturing issue in the filling equipment and has implemented corrective actions to prevent further occurrence.

MATERIAL SAFETY DATA SHEET Product Name: Heparin …

Heparin Sodium Hospira EEL N/A N/A 500 8hr TWA Respiratory protection Respiratory protection is normally not needed during intended product use. However, if the generation of aerosols is likely, and engineering controls are not considered adequate to

NDC 0409-2721 Heparin Sodium Heparin Sodium

Heparin Sodium with NDC 0409-2721 is a a human prescription drug product labeled by Hospira, Inc.. The generic name of Heparin Sodium is heparin sodium. The product's dosage form is injection, solution and is administered via intravenous; subcutaneous form. The RxNorm Crosswalk for this NDC code indicates multiple RxCUI concepts are associated ...

Hospira, Inc. HEPARIN SODIUM- heparin sodium …

HEPARIN SODIUM- heparin sodium injection, solution Hospira, Inc.-----HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use HEPARIN SODIUM INJECTION safely and effectively. See full prescribing information for HEPARIN SODIUM INJECTION. HEPARIN SODIUM INJECTION, USP for intravenous or …

Heparin Sodium (Hospira, Inc.): FDA Package Insert, Page 2

Heparin Sodium Injection is supplied in vials and sterile cartridges containing various strengths of heparin, including vials that contain a highly concentrated solution of 10,000 units in 1 mL. Fatal hemorrhages have occurred in pediatric patients due to medication errors in which 1 mL Heparin Sodium Injection vials were confused with 1 mL ...

Heparin Lock Flush Solution - FDA prescribing information ...

Heparin Lock Flush Solution, USP is a sterile, nonpyrogenic, hypertonic preparation of heparin sodium injection, USP with sodium chloride in water for injection. Each milliliter (mL) contains: Heparin sodium, 10 or 100 USP …

Hospira recalls one lot of Heparin Sodium, 1,000 USP ...

Hospira Inc. has initiated a voluntary nationwide user-level recall of one lot of Heparin Sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% Sodium Chloride Injection, 500 mL.

SAFETY DATA SHEET - Pfizer

Dalteparin Sodium (Heparin Sodium) Not Listed Not Listed 1,000, 5,000 or 10,000 USP units/mL SODIUM CHLORIDE 231-598-3 Not Listed 0.9 BENZYL ALCOHOL 100-51-6 202-859-9 Acute Tox. 4 (H302) Acute Tox. 4 (H332) 0.945 Ingredient CAS Number EU EINECS/ELINCS List

Hospira Voluntarily Recalls One Lot of Heparin for ...

Hospira, Inc is initiating a voluntary nationwide user-level recall of one lot of heparin sodium, 1,000 USP Heparin Units/500 mL (2 USP Heparin Units/mL), in 0.9% sodium chloride Injection, 500 mL, NDC 0409-7620-03 Lot 41-046-JT with an expiration date of Nov. 1, 2015.

Heparin Sodium (Hospira, Inc.): FDA Package Insert

Hospira, Inc.: Heparin Sodium Injection is indicated for: Prophylaxis and treatment of venous thrombosis and, pulmonary embolism;. Prevention of postoperative deep venous thrombosis and pulmonary...

Heparin Sodium Injection, USP - Pfizer Hospital US

Delivery Date. 01/2022. Date product is expected to arrive at Pfizer's US product distribution centers. Orders will release as deliveries arrive. All orders filled by estimated recovery date. Estimated Recovery Date. 04/2022. Date Pfizer …

Heparin Sodium in 0.9% Sodium ... - Pfizer Hospital US

Heparin Sodium in 0.9% Sodium Chloride Injection. 40301. 40306. Generic Name: Heparin Sodium in 0.9% Sodium Chloride Injection. Flexible Container (2 port) (Solution) AVAILABILITY* Image filed. UoS† NDC. CONCENTRATION. CONTENT.

NDC Code 0409-7620-13 - Heparin Sodium | …

PharmaCompass the one-stop, pharmaceutical information platform accelerates generic drug development by sharing the list of inactive ingredients used to develop Heparin Sodium marketed by Hospira, Inc. under NDC Code 0409-7620-13 …

Human Hair Discovered In Heparin Vial Prompts Hospira, …

Heparin Sodium Injection in 0.9% Sodium Chloride at a concentration of 2 units/mL is indicated as an anticoagulant to maintain catheter patency. To date, Hospira has not received reports of any adverse events associated with this issue for this lot. The root cause has not been determined and is under investigation.

HEPARIN SODIUM-FDA-

:HEPARIN SODIUM,:HEPARIN SODIUM,:090571,:HOSPIRA INC / RLD RS …

Heparin Sodium, Porcine / 0.9% Sodium Chloride ... - …

Heparin Sodium, Porcine / 0.9% Sodium Chloride, Preservative Free 2 U / mL Solution Flexible Bag 1000 mL Hospira Worldwide Inc 00409762059

HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0 ...

:HEPARIN SODIUM 5,000 UNITS IN SODIUM CHLORIDE 0.9%,:HEPARIN SODIUM,:018916,:HOSPIRA 1999/11/19 SUPPL 33 Approval Labeling STANDARD 1998/10/27 SUPPL 32 Approval Manufacturing (CMC)

Heparin 5,000 Units/mL Sodium Injection USP - Aesthetic ...

NDC Number 00409-2723-02 Manufacturer # 00409272302 Manufacturer Hospira Heparin Sodium, Porcine Strength: 5,000 U / mL Intravenous or Subcutaneous Anticoagulant Multiple Dose Vial Volume 10 mL Latex Free Indicator Not Made with …

Hospira, Inc. HEPARIN SODIUM- heparin sodium …

HEPARIN SODIUM- heparin sodium injection, solution Hospira, Inc.-----HIGHLIGHTS OF PRESCRIBING INFORMATION These highlights do not include all the information needed to use HEPARIN SODIUM IN SODIUM CHLORIDE INJECTION safely and effectively. See full prescribing information for HEPARIN SODIUM IN SODIUM CHLORIDE INJECTION.

SAFETY DATA SHEET Product Name: Heparin Sodium …

Hospira, Inc., Non-Emergency CHEMTREC: North America: 800-424-9300; International 1-703-527-3887; Australia - 61-290372994; UK - 44-870-8200418 224 212-2000 Product Name Heparin Sodium Injection, USP Synonyms None 2. HAZARD(S) IDENTIFICATION Emergency Overview Heparin Sodium Injection, USP, is a solution containing heparin sodium, a

Heparin Sodium Injection, USP - Food and Drug …

Heparin sodium may prolong the one-stage prothrombin time. Therefore, when heparin sodium is given with dicumarol or warfarin sodium, a period of at least 5 hours after the last intravenous dose or 24 hours after the last subcutaneous dose should elapse before blood is drawn, if a valid prothrombin time is to be obtained. Platelet Inhibitors

Dilution Heparin Sodium - GlobalRPH

The heparin is given by deep subcutaneous (intrafat, i.e., above the iliac crest or abdominal fat layer, arm or thigh) injection with a fine (25 to 26-gauge) needle to minimize tissue trauma. A concentrated solution of heparin sodium is recommended. Such prophylaxis should be reserved for patients over the age of 40 who are undergoing major ...

Hospira, Inc. - List of Drugs - NDC Labeler/Manufacturer

Hospira, Inc. 00409-7993. Potassium Chloride in Dextrose and Sodium Chloride. Hospira, Inc. 00409-7998. Potassium Chloride in Dextrose and Sodium Chloride. Hospira, Inc. 00409-7111. Potassium Chloride in Lactated Ringers and Dextrose.

Heparin products | Therapeutic Goods Administration (TGA)

As a result of these reports the TGA has tested all brands of heparin sodium available on the Australian market for the detection of the contaminant. The TGA has completed its testing of heparin sodium products currently distributed in …

URGENT: Important Safety Information - Food and Drug ...

Hospira, a Pfizer company (Hospira) is issuing this Important Safety Information Letter to alert ... 0409-1316-32 Heparin Sodium Injection, USP, 5,000 USP Heparin Units/0.5 mL in 2.5 mL Carpuject ...

Version 1.02 Page 1 / 10 - Pfizer

Product Name Heparin Sodium in 5% Dextrose Injection (Hospira, Inc.) Product Code(s) PZ03548 Trade Name: Heparin Sodium in 5% Dextrose Injection Chemical Family: Mixture 1.2. Relevant identified uses of the substance or mixture and uses advised against Recommended Use Pharmaceutical product used as anticoagulant agent 1.3.

SAFETY DATA SHEET Product Name: Heparin Lock Flush ...

Active Ingredient Name Heparin Sodium Chemical Formula Heparin is an acidic, polymeric mucopolysaccharide composed of units of glucuronic acid and sulfated glucosamine Component Approximate Percent by Weight CAS Number RTECS Number Heparin Sodium < 0.1% MI0850000 Non-hazardous ingredients include Water for Injection.