D.K. Pharmachem Pvt. Ltd.

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Buclizine Hydrochloride API Manufacturer & Exporter

WHO-GMP certified bulk Buclizine HCl supplier for global pharmaceutical formulators

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Buclizine hydrochloride molecular structure illustrating its chemical composition and antihistamine classification

D.K. Pharmachem Pvt. Ltd. is among India’s trusted buclizine hydrochloride API manufacturers, supplying high-quality buclizine HCl for pharmaceutical formulations. Buclizine Hydrochloride is widely used as an antiemetic API, commonly formulated into buclizine hydrochloride tablets for the treatment of nausea, vomiting and motion sickness.

With decades of experience in API manufacturing, we cater to domestic and international markets with consistent quality, regulatory compliance and reliable bulk supply.

Buclizine Hydrochloride API Specifications | CAS 129-74-8

Attribute Details
Pharmacopoeia Standard USP / EP
CAS Number 129-74-8
Molecular Formula C₂₈ H₃₃ Cl N₂ . 2HCl
Molecular Weight 505.95 g/mol
Therapeutic Application Antihistamine & Antiemetic
DMF / EDMF Status Available
Manufacturing Standard WHO-GMP Certified
Appearance White to off-white crystalline powder
Purity ≥99% (HPLC)

Manufacturing Capabilities & Supply Strength

Buclizine Hydrochloride API at DK Pharmachem is manufactured through a controlled chemical synthesis process, where reaction parameters - temperature, solvent selection, pH, and crystallisation conditions - are carefully validated to ensure consistent purity and reproducibility across every batch. Our WHO-GMP certified facility in Badlapur, Maharashtra operates dedicated production streams for API synthesis, with in-house quality control laboratories equipped with HPLC, GC, IR, UV, and Karl Fischer systems for comprehensive batch testing.

Advanced infrastructure for buclizine dihydrochloride and buclizine HCl synthesis

Dedicated production lines ensuring batch-to-batch consistency

In-house quality control and analytical testing

Scalable capacity for bulk buclizine HCl supply

Reliable sourcing for pharmaceutical formulation manufacturers

Comprehensive documentation

Comprehensive documentation support including DMF and regulatory filings

As one of the established buclizine hydrochloride API manufacturers in India, we ensure uninterrupted supply chains and strict adherence to global quality standards.

Why Pharmaceutical Companies Source Bulk Buclizine HCl from India

Stringent regulatory environment

Indian API manufacturers operate under CDSCO oversight and are eligible for WHO-GMP, US FDA, EU GMP, and PMDA certifications, giving procurement teams confidence that quality standards meet their market requirements

Cost-competitive without quality compromise

India’s established API supply chain and skilled workforce deliver globally competitive pricing on Buclizine HCl without compromising on purity or documentation standards

Proven export infrastructure

India exports APIs to over 200 countries, with established logistics, customs expertise, and documentation experience for regulated and semi-regulated markets across Asia-Pacific, Africa, the Middle East, Latin America, and Europe

Backward integration advantage

Indian manufacturers with in-house intermediate synthesis offer supply chain resilience that import-dependent suppliers cannot, directly reducing raw material risk for your procurement team

Scale and supply continuity

India’s pharmaceutical manufacturing base is large enough to absorb demand fluctuations without compromising lead times, making it a dependable long-term sourcing region for APIs like Buclizine HCl

Buclizine hydrochloride API manufacturing facility with cleanroom production and industrial processing systems

Bulk Supply, Packaging Options & Export Logistics

DK Pharmachem supplies Buclizine Hydrochloride API in flexible pack sizes to meet the requirements of both development-stage and commercial-scale pharmaceutical manufacturers. Standard packaging is available in 1 kg, 5 kg, and 25 kg HDPE drums with double-polyethylene inner lining to ensure protection from moisture and contamination throughout transit. Custom packing configurations are available on request.

We export Buclizine HCl API to pharmaceutical manufacturers across Asia-Pacific, the Middle East, Africa, Latin America, and Europe. Standard lead times from order confirmation are 10-15 working days for stocked material; for larger custom batches, our team will advise on specific timelines at enquiry stage. All export shipments are accompanied by a full documentation pack - Certificate of Analysis, MSDS, and any additional regulatory documents required for your destination market.

For Pharmaceutical Manufacturers & Research Labs

Partner with a WHO-GMP certified supplier for consistent quality, regulatory compliance, and reliable supply of Buclizine Hydrochloride for your critical applications.

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Why Choose DK Pharmachem for Buclizine Hydrochloride

Choosing the right API partner is critical for product quality and regulatory success.

Leading buclizine hydrochloride API manufacturer and exporter

Proven expertise in antiemetic APIs

Strong compliance with international quality standards

Competitive pricing for bulk buclizine HCl suppliers

Transparent documentation and technical support

Long-term reliability backed by decades of manufacturing experience

D.K. Pharmachem is trusted by pharmaceutical companies for consistent quality and dependable supply.
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Frequently Asked Questions for Buclizine Hydrochloride

Find answers to common questions about Buclizine Hydrochloride products and services

What is the minimum order quantity for Buclizine Hydrochloride API?

DK Pharmachem supplies Buclizine HCl API from 1 kg upwards for research and development purposes. For commercial bulk orders, standard pack sizes are 5 kg and 25 kg. Custom volumes and packaging configurations are available – contact our team with your specific quantity and timeline requirements.
Yes. DK Pharmachem’s API manufacturing facility is WHO-GMP certified and operates in full compliance with current Good Manufacturing Practice (cGMP) standards. Our facility is regularly audited by domestic and international pharmaceutical clients and regulatory bodies.
DK Pharmachem’s Buclizine Hydrochloride API is manufactured to conform to BP (British Pharmacopoeia) and IP (Indian Pharmacopoeia) standards. Custom specifications to meet other pharmacopoeial requirements can be discussed on enquiry.
DK Pharmachem exports Buclizine HCl API to pharmaceutical manufacturers across Asia-Pacific, the Middle East, Africa, Latin America, and Europe. We have experience supplying to both regulated markets (requiring comprehensive documentation packages) and semi-regulated markets. Contact us with your destination country for specific documentation requirements.
Yes. Every batch of Buclizine Hydrochloride API dispatched from DK Pharmachem is accompanied by a Certificate of Analysis covering identity, assay, impurity profile, physical characteristics, and storage conditions. MSDS and other regulatory documents are available on request.
Yes. DK Pharmachem provides analytical samples of Buclizine Hydrochloride API for qualification purposes prior to bulk ordering. To request a sample, please contact our team via the enquiry form with your company details, intended application, and required quantity. Our team typically responds within 1-2 working days.