Pharmaceutical sterile vials and water for injection
Manufacturer & Global Supplier

India's Biggest Manufacturer &
Global Supplier of
Bacteriostatic Water
For Injection

A premium B2B pharmaceutical supplier delivering reliable bacteriostatic water for injection with batch traceability, consistent quality, and export-focused fulfillment.

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Bacteriostatic water vials

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Sterile Manufacturing
Batch Traceability
Export Supply
B2B Focused
Quality Documentation
Timely Dispatch
Laboratory environment
Understanding the Product

What is Bacteriostatic Water
For Injection?

Bacteriostatic Water for Injection, USP is a sterile, nonpyrogenic preparation of Water for Injection containing 0.9% benzyl alcohol as a bacteriostatic preservative.

It is supplied in a multiple-dose plastic container and is intended for use as a sterile diluent in the preparation of parenteral solutions. The benzyl alcohol inhibits the growth of most contaminating organisms, allowing the container to be used repeatedly for up to 28 days after initial entry.

This formulation is manufactured to meet the rigorous standards of the United States Pharmacopeia (USP), ensuring pharmaceutical-grade purity, controlled pH levels between 4.5 and 7.0, and freedom from endotoxins.

Sterile vials in laboratory
USP-Grade Sterile Preparation
01

Bacteriostatic Preservative

Contains 0.9% benzyl alcohol that inhibits bacterial growth in multi-dose vials.

02

Multi-Dose Capability

Allows repeated withdrawals from a single vial over an extended period.

03

Pharmaceutical Diluent

Used to dilute or dissolve drugs for intravenous, intramuscular, or subcutaneous injection.

04

Controlled pH Range

Maintained within 4.5 to 7.0 for optimal compatibility with injectable formulations.

Technical Details

Product Specifications

Comprehensive technical data for pharmaceutical procurement teams and regulatory professionals.

Composition

Water for Injection, USP with 0.9% (9 mg/mL) benzyl alcohol as a bacteriostatic preservative.

pH Range: 4.5 – 7.0

Sterility

Manufactured under controlled aseptic conditions meeting current Good Manufacturing Practice (cGMP) standards.

Nonpyrogenic: Yes

Presentation

Available in multi-dose vials and bulk supply formats for domestic and international markets.

Formats: Custom available

Packaging

Custom packaging solutions for domestic and export buyers with tamper-evident sealing.

Export-Ready: Yes

Storage

Store at controlled room temperature, 20°C to 25°C (68°F to 77°F). Protect from light.

Shelf Life: Per labeling

Use Case

Pharmaceutical diluent for reconstitution of injectable drugs per manufacturer directions.

Route: IV, IM, SC
Our Advantage

Built for Reliability,
Scale & Global Supply

We combine pharmaceutical-grade manufacturing discipline with responsive B2B service for partners who demand consistency.

01

Controlled Manufacturing

Every batch is produced in a controlled environment with validated processes, ensuring consistent quality from raw material to finished product.

02

Consistent Batch Quality

Stringent in-process and final quality checks guarantee that every unit meets pharmaceutical-grade specifications and USP compliance.

03

Documentation Support

Complete COA, MSDS, and product documentation available on request. We support your regulatory submissions with accuracy.

04

Export Packaging

Designed for international logistics with secure, compliant packaging that maintains product integrity across global supply chains.

05

Responsive B2B Sales

Dedicated B2B support team ensuring rapid response to inquiries, transparent communication, and reliable order tracking.

06

Flexible Order Volumes

From trial orders to full container loads, we accommodate varying volumes with the same quality commitment and service standards.

Process & Standards

Manufacturing &
Quality Standards

Our production process follows disciplined aseptic manufacturing protocols, ensuring every batch of Bacteriostatic Water for Injection meets the highest pharmaceutical quality benchmarks.

Controlled production environment
In-process and final quality checks
Batch coding and full traceability
COA / MSDS / documentation support
Export-ready packing and dispatch
01
Raw material control

Raw Material Control

Pharmacopeia-grade Water for Incoming inspection, testing, and certified storage.

02
Sterile manufacturing

Sterile Manufacturing

Aseptic compounding with benzyl alcohol preservative under validated cleanroom conditions.

03
Quality testing

Quality Testing

Sterility, endotoxin, pH, particulate, and preservative effectiveness testing.

04
Batch release

Batch Release

Quality assurance review with full batch documentation and Certificate of Analysis.

05
Packing and dispatch

Packing & Export Dispatch

Tamper-evident packaging with temperature-controlled logistics for international shipment.

Quality laboratory
Quality Assurance

Precision in Every Batch

Cleanroom production

Aseptic Processing

Manufactured in controlled environments with validated aseptic processes to ensure product sterility.

Quality testing lab

Analytical Testing

Comprehensive testing protocols including sterility, endotoxin, pH, and particulate matter analysis.

Documentation and compliance

Documentation

Complete batch records, Certificates of Analysis, and MSDS provided with every order.

Global Reach

Serving Domestic &
International Buyers

We supply Bacteriostatic Water for Injection to pharmaceutical distributors, hospitals, and healthcare institutions across multiple countries.

North America

North America

Serving pharmaceutical distributors and healthcare institutions across the United States and Canada.

Europe

Europe

Reliable supply supporting pharmaceutical markets across the European Union and surrounding regions.

Latin America

Latin America

Supporting growing healthcare infrastructure with consistent pharmaceutical-grade supply.

Australia

Australia & Oceania

Export partnerships serving pharmaceutical demand across Australia and the Pacific region.

Important Product Note

Bacteriostatic Water for Injection is intended for use as a sterile diluent in the preparation of parenteral solutions, according to manufacturer directions. It is not for use in neonates due to benzyl alcohol toxicity risk. Intravenous administration without a solute may cause hemolysis. This product should not be used as a fluid replacement. Always follow applicable labeling and regulatory requirements. (DailyMed Reference)

Get in Touch

Request a Quote

Whether you need product specifications, pricing, MOQ details, or export documentation — our B2B team is ready to assist.

sales@bacwatersupplier.com
+91 XXXXX XXXXX
Manufacturing Facility, Gujarat, India
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Instant response during business hours

Response for bulk and export inquiries within business hours.