Anti-Infective APIs / Penicillin Antibiotic & Beta-Lactamase Inhibitor APIs

Product Type

Sterile Active Pharmaceutical Ingredient (Sterile API)

CAS Number

61477-96-1 (Piperacillin Sodium)

Regulatory File Status

• USDMF Available*
• EDMF Available*

*Availability is subject to the selected manufacturing partner and applicable regulatory requirements.

Product Name

Piperacillin Sodium and Tazobactam Sodium Active Pharmaceutical Ingredient (API)

Product Overview

Piperacillin Sodium and Tazobactam Sodium is a Sterile Active Pharmaceutical Ingredient (Sterile API) consisting of Piperacillin Sodium, a broad-spectrum ureidopenicillin antibiotic, and Tazobactam Sodium, a beta-lactamase inhibitor. This pharmaceutical combination is widely used in the manufacture of sterile injectable anti-infective formulations, providing broad-spectrum antibacterial activity while protecting Piperacillin from degradation by beta-lactamase-producing microorganisms.

The API combination is sourced through qualified pharmaceutical manufacturing partners while complying with applicable quality, pharmacopoeial, sterile manufacturing, and regulatory standards.

BLUEPILL EXPORT is a trusted merchant exporter and pharmaceutical sourcing partner specializing in the global sourcing and supply of sterile pharmaceutical APIs, penicillin antibiotics, beta-lactamase inhibitor APIs, injectable pharmaceutical ingredients, pharmaceutical intermediates, excipients, and pharmaceutical raw materials. We act as a reliable intermediary between qualified pharmaceutical manufacturers and licensed international buyers by providing procurement support, export documentation, manufacturer coordination, and comprehensive pharmaceutical supply chain solutions.

Through our extensive network of qualified pharmaceutical manufacturing partners, we support sterile injectable manufacturers, pharmaceutical companies, biotechnology companies, contract manufacturing organizations (CMOs), research institutions, pharmaceutical importers, distributors, and procurement agencies worldwide.

Key Features of Piperacillin Sodium and Tazobactam Sodium API

• Sterile Active Pharmaceutical Ingredient (Sterile API)
• Piperacillin Sodium and Tazobactam Sodium combination
• USDMF Available*
• EDMF Available*
• Broad-spectrum ureidopenicillin antibiotic with beta-lactamase inhibitor
• Pharmaceutical-grade sterile material
• Suitable for injectable pharmaceutical formulation development
• Batch-specific quality documentation available
• Commercial and development-scale sourcing support
• Reliable sourcing through qualified pharmaceutical manufacturing partners
• Export documentation support

Pharmaceutical Applications

Piperacillin Sodium and Tazobactam Sodium API is commonly utilized in:

• Sterile injectable antibiotic formulations
• Combination anti-infective pharmaceutical products
• Injectable powder formulations
• Hospital injectable products
• Generic pharmaceutical development
• Pharmaceutical research and development
• Commercial pharmaceutical manufacturing
• Beta-lactam antibiotic combination products

Pharmaceutical Sourcing Services

BLUEPILL EXPORT provides comprehensive pharmaceutical sourcing solutions, including:

• Global sterile API sourcing
• Merchant export services
• Pharmaceutical procurement support
• Manufacturer identification and coordination
• Third-party manufacturing coordination
• Contract manufacturing assistance
• Export documentation support
• International logistics coordination
• Supply chain management
• Long-term procurement partnerships

Why Choose BLUEPILL EXPORT?

• Trusted merchant exporter for sterile pharmaceutical APIs
• Extensive network of qualified pharmaceutical manufacturing partners
• Reliable sourcing for regulated and semi-regulated pharmaceutical markets
• Professional procurement assistance
• Complete export documentation support
• Transparent communication throughout the sourcing process
• Flexible sourcing for commercial and development quantities
• Dedicated customer support
• Efficient international logistics coordination

Documentation Support

Documentation availability depends on the selected manufacturing partner and customer qualification requirements.

Typical documentation may include:

• Certificate of Analysis (COA)
• Material Safety Data Sheet (MSDS)
• Technical Data Sheet (TDS)
• Certificate of Origin
• GMP Documentation (where applicable)
• USDMF Reference Support (where authorized)
• EDMF Reference Support (where authorized)
• Sterility Certificate (where applicable)
• Stability Data (where available)
• Commercial Invoice
• Packing List
• Shipping Documentation

Packaging Information

Packaging options are arranged according to the selected manufacturing partner’s sterile packaging specifications and customer requirements while complying with applicable international transportation and export regulations.

Industries We Serve

• Sterile Injectable Manufacturers
• Pharmaceutical Manufacturers
• Biotechnology Companies
• Contract Manufacturing Organizations (CMOs)
• Pharmaceutical Importers
• Pharmaceutical Distributors
• International Pharmaceutical Trading Companies
• Pharmaceutical Procurement Agencies

Contact BLUEPILL EXPORT

For product availability, technical documentation, sourcing support, or export inquiries, please contact:

BLUEPILL EXPORT

Email: info@bluepillexport.com

Important Notice

BLUEPILL EXPORT operates exclusively as a merchant exporter and pharmaceutical sourcing partner. We facilitate global sourcing through our network of qualified pharmaceutical manufacturing partners. Product availability, specifications, documentation, formulation ratios, and regulatory support are subject to the selected manufacturing partner and applicable regulatory requirements.

References to USDMF and EDMF indicate that applicable regulatory documentation may be available through the selected manufacturing partner where authorized. Such references do not imply regulatory approval or endorsement by BLUEPILL EXPORT.

This product is intended solely for pharmaceutical manufacturing, research, formulation development, and other authorized industrial applications in accordance with applicable laws and regulations.