Tamoxifen Citrate pharmaceutical API powder — CAS 54965-24-1 — WHO-GMP manufacturer Longshine Boi-Tech, Pune, India
Human APIs

Tamoxifen Citrate

CAS Registry Number: 54965-24-1

Tamoxifen Citrate is a selective estrogen receptor modulator (SERM) used primarily in the adjuvant treatment of ER-positive breast cancer and for chemoprevention in high-risk populations. Manufactured to USP and Ph. Eur. monograph specifica

Product information

Tamoxifen Citrate is a selective estrogen receptor modulator (SERM) used primarily in the adjuvant treatment of ER-positive breast cancer and for chemoprevention in high-risk populations. Manufactured to USP and Ph. Eur. monograph specifications with full impurity profile per ICH Q3A/M7. Longshine Boi-Tech maintains active regulatory filings including US FDA Type II DMF and EDQM CEP references for qualified buyers.

Product specifications

CAS Registry Number
54965-24-1
Therapeutic Category
Human APIs
API Technology
Synthetic / Semi-synthetic (per molecule)
Development Status
Commercial — stocked
Manufacturer
Longshine Boi-Tech Pvt. Ltd.
Facility
Pune, Maharashtra, India 411001

Regulatory filings & documentation

We maintain regulatory dossiers in the following jurisdictions for Tamoxifen Citrate-relevant molecules. Letter of Authorization (LoA) and CEP / DMF / ASMF references are issued at no charge to qualified buyers.

US FDA DMF (Type II)
EDQM CEP (where applicable)
Brazil ANVISA
Canada Health Canada
Japan PMDA
Korea MFDS
GCC SFDA
EU CEP
WHO-GMP & ISO 9001:2015 certified. US FDA Drug Master File available. EDQM CEP supplied for EU procurement. Pharmacopoeial release against USP, Ph. Eur., IP, JP. CoA on every batch. First-shipment lead time 7-10 business days for stocked APIs.
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Frequently asked questions about Tamoxifen Citrate

What is Tamoxifen Citrate used for?

Tamoxifen Citrate is supplied as a pharmaceutical-grade human apis for use by regulated pharmaceutical manufacturers, contract development and manufacturing organisations (CDMOs), and research institutions. Buyers using Tamoxifen Citrate typically reference it under CAS Registry Number 54965-24-1.

What quality and regulatory standards does Longshine Boi-Tech's Tamoxifen Citrate meet?

Our Tamoxifen Citrate is manufactured under WHO-GMP and ISO 9001:2015 conditions in Pune, India. Per-batch Certificate of Analysis (CoA) is released against USP / Ph. Eur. / IP / JP specifications depending on destination market. We hold US FDA Drug Master File and EDQM Certificate of Suitability dossiers for the molecules where regulatory recognition is required; Letter of Authorization (LoA) is issued at no charge to qualified buyers.

How do I request a quote, sample, or proforma invoice for Tamoxifen Citrate?

Quote requests for Tamoxifen Citrate are turned around within 24 business hours (IST, Pune). Bulk APIs typically ship within 7-10 business days of confirmed PO; air freight to North America and Europe runs 4-5 days door-to-door. Sample agreements are signed before shipping QC-grade material to your formulation laboratory.

Which countries does Longshine Boi-Tech supply Tamoxifen Citrate to?

We export Tamoxifen Citrate to 50+ countries including the United States, Canada, Mexico, Brazil, the European Union, the United Kingdom, Japan, Australia, South Korea, the GCC and across South-East Asia. All regulatory documents (DMF / CEP / LoA) and shipping incoterms (EXW, FCA, CIP, DAP, DDP) are negotiated per buyer.

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Related categories & resources

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