Water (Sterile Water)

Trade Name : Sterile Water

B. Braun Medical Inc.

INJECTION

Strength 1 mL/mL

WATER

Delivery Process

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You can fill in a request for your medicine through the form provided. You can access the form by clicking on the ‘Get Price’ button.

Product information is meant for

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Disclaimer

Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Water (Sterile Water) which is also known as Sterile Water and Manufactured by B. Braun Medical Inc.. It is available in strength of 1 mL/mL per ml. Read more

Water (Sterile Water) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

Packaging and Delivery

Validated Cold Chain Shipment

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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About GNH

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

Read more
  • No data
  • Warning: Hypotonic and hemolytic.Do not inject until made approximately isotonic by addition of appropriate solute.
  • Pharmacy Bulk PackageNot For Direct Infusion
  • Sterile Water for Injection USP is a clear, colorless, odorless liquid. It is sterile, hypotonic, nonpyrogenic, and contains no bacteriostatic or antimicrobial agents. Sterile Water for Injection USP is a diluent suitable for intravascular injection after first having been made approximately isotonic by the addition of suitable solute.
  • pH: 5.5 (5.0-7.0)
  • Not made with natural rubber latex, PVC or DEHP.
  • The plastic container is made from a multilayered film specifically developed for parenteral drugs. It contains no plasticizers and exhibits virtually no leachables. The solution contact layer is a rubberized copolymer of ethylene and propylene. The container is nontoxic and biologically inert. The container-solution unit is a closed system and is not dependent upon entry of external air during use. The container is overwrapped to provide protection from the physical environment and to provide an additional moisture barrier when necessary.
  • Sterile Water for Injection USP is used as a diluent for other parenteral drugs. As such, Sterile Water for Injection USP contributes to the water for hydration when provided in parenteral drug and fluid therapy, after the introduction of suitable additives and/or mixture with suitable solutes to approximate isotonicity.
  • Sterile Water for Injection USP is indicated for use in adults and pediatric patients as a diluent in the aseptic preparation of parenteral solutions or as a vehicle for drug administration after admixture or dilution.
  • None known.
  • This solution is for compounding only, not for direct infusion.
  • Hypotonic and hemolytic.
  • The administration of intravenous solutions can cause fluid and/or solute overload resulting in dilution of serum electrolyte concentrations, overhydration, congested states or pulmonary edema. The risk of dilutional states is inversely proportional to the electrolyte concentration.
  • WARNING: This product contains aluminum that may be toxic. Aluminum may reach toxic levels with prolonged parenteral administration if kidney function is impaired. Premature neonates are particularly at risk because their kidneys are immature, and they require large amounts of calcium and phosphate solutions, which contain aluminum.
  • Research indicates that patients with impaired kidney function, including premature neonates, who receive parenteral levels of aluminum at greater than 4 to 5 mcg/kg/day accumulate aluminum at levels associated with central nervous system and bone toxicity. Tissue loading may occur at even lower rates of administration.
  • No data
  • Refer to the package insert of the solute used.
  • Reactions which may occur because of the solution or the technique of administration include febrile response, infection at the site of injection, venous thrombosis or phlebitis extending from the site of injection, extravasation and hypervolemia.
  • The physician should also be alert to the possibility of adverse reactions to drug additives. Prescribing information for drug additives to be administered in this manner should be consulted.
  • If an adverse reaction does occur, discontinue the infusion, evaluate the patient, institute appropriate therapeutic countermeasures and save the remainder of the fluid for examination if deemed necessary.
  • Overdosage (hypotonic expansion) is a function of an increase in fluid intake over fluid output, and occurs when the increase in the volume of body fluids is due to water alone. Overdosage may occur in patients who receive large quantities of electrolyte-free water to replace abnormal excessive fluid losses, in patients whose renal tolerance to water loads is exceeded, or in patients who retain water postoperatively in response to stress.
  • Manifestations of water intoxication are behavioral changes (confusion, apathy, disorientation and attendant hyponatremia), central nervous system disturbances (weakness, muscle twitching, headaches, nausea, vomiting, convulsions) and weight gain.
  • Treatment consists of withholding fluids until excessive water is excreted. In severe hyponatremia it may be necessary to cautiously administer hypertonic saline to increase extracellular osmotic pressure and excretion of excess water by the kidneys.
  • This solution is for intravenous use only after admixture or dilution. Do not inject until made approximately isotonic by addition of appropriate solute.
  • Following suitable admixture of prescribed drugs, the dosage is usually dependent upon the age, weight and clinical condition of the patient as well as laboratory determinations. See directions accompanying drugs.
  • The dosage and administration of Sterile Water for Injection USP is dependent upon the recommended dosage and administration of the solute used. Fluid administration should be based on calculated maintenance or replacement fluid requirements for each patient.
  • Some additives may be incompatible. Consult with pharmacist. When performing admixture or dilution, use aseptic techniques. Mix thoroughly. Do not store.
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration, whenever solution and container permit.
  • Sterile Water for Injection USP is supplied in 2000 and 3000 mL Pharmacy Bulk Package containers packaged 4 per case.
  • Exposure of pharmaceutical products to heat should be minimized. Avoid excessive heat. Protect from freezing. It is recommended that the product be stored at room temperature (25u00b0C); however, brief exposure up to 40u00b0C does not adversely affect the product.
  • Rx only
  • Revised:u00a0May 2019
  • Warning: Hypotonic and hemolytic. Do not inject until made approximately isotonic by addition of appropriate solute.
  • Parenteral drug products should be inspected visually for particulate matter and discoloration prior to administration and final infusate should be inspected for cloudiness or precipitation immediately after mixing, prior to administration, and periodically during administration, whenever solution and container permit. Use of a final filter is recommended during administration of all parenteral solutions where possible.
  • Sterile Water for Injection USP in the Pharmacy Bulk Package is intended for use in the preparation of sterile, intravenous admixtures. Additives may be incompatible with the fluid withdrawn from this container. Complete information is not available. Those additives known to be incompatible should not be used. Consult with pharmacist, if available.
  • When compounding admixtures, use aseptic technique. Mix thoroughly.
  • Do not store any unused portion of Sterile Water for Injection USP.
  • Arrayn- Preparationn n
  • 1.u00a0 To open: Tear overwrap starting from the tear notches. (Figure 1)n n
  • Arrayn- For Pharmacy Bulk Packages
  • Arrayn- Important Admixing Instructions
  • B. Braun Medical Inc.
  • Y36-002-998u00a0 LD-454-2
  • Sterile Water for Injection USP
  • Arrayn- Array
  • REF S8505n n- NDC 0264-7385-50n n- LOTn n- EXP.
  • 2000 mL
  • Pharmacy Bulk Packagen n- Not For Direct Infusionn
  • No antimicrobial agent or other substance has been added.
  • Sterile. Pharmacy bulk package container.
  • WARNINGS:
  • CONTAINS NO MORE THAN 25 mcg/L OF ALUMINUM
  • Recommended Storage: Room temperature (25u00b0C). Avoid excessive heat. Protect from freezing. Do not remove overwrap until ready for use. Once container closure has been penetrated, withdrawal of content should be completedwithin 4 hours. See Package Insert.
  • Not made with natural rubber latex, PVC or DEHP.u00a0
  • Rx only
  • Arrayn- Array
  • Y38-000-053u00a0u00a0u00a0u00a0 LD-455-2
  • SET
  • Arrayn- Array
  • Sterile Water for Injection USP
  • Arrayn- Array
  • REF S8506n n- NDC 0264-7385-60n n- LOTn n- EXP.
  • 3000 mL
  • Pharmacy Bulk Packagen n- Not For Direct Infusion
  • No antimicrobial agent or other substance has been added.
  • Sterile. Pharmacy bulk package container.
  • WARNINGS:
  • CONTAINS NO MORE THAN 25 mcg/L OF ALUMINUM
  • Recommended Storage: Room temperature (25u00b0C). Avoid excessive heat. Protect from freezing. Do not remove overwrap until ready for use.u00a0Once containerclosure has been penetrated, withdrawal of content should be completed within 4 hours. See Package Insert.
  • Not made with natural rubber latex, PVC or DEHP.u00a0
  • Rx only
  • Arrayn- Array
  • Y38-000-054u00a0u00a0u00a0u00a0 LD-456-2
  • SET
  • Arrayn- Array

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