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Oritavancin Diphosphate bulk supplier for pharma manufacturers

Oritavancin Diphosphate Suppliers & Bulk Manufacturers

Available Forms: Injection

Available Strengths: 400 mg

Reference Brands: Orbactiv (USA)

Category: Antibiotics

Oritavancin Diphosphate is available in Injection and strengths such as 400 mg. Sourced from GMP-certified and ISO-compliant manufacturers, this API meets global pharmacopeia standards (USP/EP/JP as applicable). Ideal for pharmaceutical formulation and commercial manufacturing, Oritavancin Diphosphate is supplied in bulk quantities with complete regulatory support including DMF, COA, and MSDS.

Technical Specifications & Supply Details
Lead Time 7 to 60 days (depending on batch size & schedule)
MOQ As per manufacturer’s batch size
COA Available with every batch
Regulatory Dossier / DMF Available upon request
Export Documentation FSC, COA, Manufacturing License, Product Permission
Standards IP, BP, USP
Certifications WHO-GMP, EU-GMP, USFDA (as applicable)

Oritavancin Diphosphate can be exported to over 30 countries across Asia, Africa, Europe, and Latin America. Flexible packaging, competitive pricing, and a verified supplier network make Pharmatradz a trusted sourcing partner for pharmaceutical companies and contract manufacturers worldwide.

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📘 Sourcing Guide

Product Description:

Oritavancin, marketed under the brand name Orbactiv, is a semisynthetic glycopeptide antibiotic used for the treatment of serious Gram-positive bacterial infections, including methicillin-resistant Staphylococcus aureus (MRSA). Structurally related to vancomycin, it is a lipoglycopeptide that inhibits bacterial cell wall synthesis and disrupts membrane integrity, leading to rapid bacterial cell death.

Oritavancin is considered a long-acting antibiotic due to its extended half-life of up to 16 days and high plasma protein binding (~85%), which allows for sustained therapeutic concentrations in tissues. The drug demonstrates excellent tissue penetration, including skin structures, synovial fluid, bone tissue, and macrophages, making it effective in treating complex infections. Its pharmacokinetic properties enable less frequent dosing while maintaining potent activity against Gram-positive pathogens.

These features make oritavancin a convenient option for outpatient therapy, particularly in populations where adherence may be challenging or access to healthcare is limited. It is suitable for prolonged courses in infections such as osteoarticular infections, endocarditis, and other deep-seated Gram-positive infections. Oritavancin should be administered under specialist supervision to ensure optimal efficacy and patient safety.

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Frequently Asked Questions

Oritavancin diphosphate is used to treat acute bacterial skin and skin structure infections (ABSSSI) caused by susceptible Gram-positive bacteria, including MRSA.

Oritavancin diphosphate is a semisynthetic lipoglycopeptide antibiotic derived from a naturally occurring glycopeptide compound, formulated as a sterile injectable powder.

The trade name is Orbactiv.

Orbactiv is marketed by Melinta Therapeutics (USA).

The complete generic name is oritavancin diphosphate.

The approved brand name is Orbactiv.

Oritavancin diphosphate is manufactured in GMP-approved facilities in the USA and other regulated pharmaceutical manufacturing regions, depending on the authorized supplier.

Yes, Oritavancin Diphosphate is available with DMF and other regulatory documents such as COA and MSDS. These can be provided upon request for qualified buyers.

Absolutely. Sample requests are accepted for formulation trials and quality checks. Please submit an enquiry to initiate the process.

Our manufacturing partners are GMP-certified and comply with ISO and WHO standards, ensuring global quality benchmarks.

Lead times vary based on quantity and destination, but most orders are fulfilled within 1–3 weeks. Express shipping options are available.

Yes, Oritavancin Diphosphate is exported to over 30 countries across Asia, Africa, Europe, and Latin America. We support documentation for customs and regulatory clearance.

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