Active Pharmaceutical Ingredient

Octreotide (CAS 79517-01-4) API Manufacturer & Supplier in India

Also known as: Sandostatin; Longastatin

CAS: 79517-01-4 Somatostatin Analogue / Peptide API IP / BP / EP / USP GMP Certified Aurangabad, Maharashtra, India
Octreotide API — Mediocon Inc
Octreotide — Pharmaceutical Grade API

Product Overview

CAS No: 79517-01-4  |  MF: C₄₉H₆₆N₁₀O₁₀S₂  |  MW: 1019.24 g/mol

Octreotide is a pharmaceutical-grade active ingredient classified as Somatostatin Analogue / Peptide API. Mediocon Inc supplies high-purity Octreotide API conforming to IP / BP / EP / USP specifications, manufactured in our GMP-certified facility in Aurangabad, Maharashtra, India.

Octreotide is a synthetic somatostatin analogue used in the management of acromegaly, carcinoid tumors, and severe diarrhea associated with VIPomas.

Key Features

  • Somatostatin analogue peptide
  • IP/BP/EP/USP compliant
  • Full CoA and MSDS documentation
  • GMP certified manufacturing

Applications

  • Acromegaly treatment
  • Carcinoid tumors
  • VIPomas
  • Esophageal variceal bleeding

Why Choose Mediocon

  • ISO 9001:2015 & GMP certified manufacturing
  • Consistent batch-to-batch quality with full CoA
  • Export-ready documentation: COO, MSDS, DMF
  • Flexible MOQ for both R&D and commercial scale
  • Dedicated QA support for regulatory filings

Product Specifications

Product NameOctreotide
Also Known AsSandostatin; Longastatin
CAS Number79517-01-4
Molecular FormulaC₄₉H₆₆N₁₀O₁₀S₂
Molecular Weight1019.24 g/mol
CategorySomatostatin Analogue / Peptide API
AppearanceWhite to off-white lyophilized powder
SolubilitySoluble in water
GradeIP / BP / EP / USP

Analytical Specifications

ParameterSpecification
AssayNLT 98.0%
Loss on DryingNMT 0.5%
Heavy MetalsNMT 20 ppm
Residue on IgnitionNMT 0.1%
Microbial LimitsComplies with pharmacopoeia
IdentificationIR, HPLC Compliant
Packing25 kg HDPE drums / as per requirement

Sourcing, Regulatory & Export Information

Mediocon Inc is a GMP-certified API manufacturer and bulk pharmaceutical ingredient supplier based in Aurangabad, Maharashtra, India. We specialise in supplying Octreotide (CAS 79517-01-4) and over 1,000 other Active Pharmaceutical Ingredients, excipients, herbal extracts, and nutraceutical ingredients to pharmaceutical manufacturers worldwide.

Our Octreotide is manufactured under strict quality management protocols compliant with WHO-GMP, ISO 9001:2015, and major pharmacopoeial standards (IP, BP, USP, EP). Every batch undergoes full analytical testing — identity (IR/HPLC), assay, related substances, residual solvents (ICH Q3C), heavy metals, and microbial limits — before release with a Certificate of Analysis.

Export Markets

  • USA — FDA-registered facility; DMF support available for ANDA/NDA filings
  • Europe — EMA-compliant documentation; CEP/EDMF support on request
  • Africa & Middle East — WHO-GMP certified; competitive pricing for emerging markets
  • Southeast Asia — established logistics network; temperature-controlled shipments
  • India domestic — schedule H/X compliance; all state licensing documentation provided

Quality & Compliance

  • ISO 9001:2015 certified quality management system
  • GMP-certified manufacturing facility, Aurangabad, Maharashtra
  • Full batch traceability from raw material to finished API
  • Stability data available (ICH Q1A guidelines) for regulatory submissions
  • Dedicated QA team for customer audits and regulatory queries

Frequently Asked Questions — Octreotide API

What is the minimum order quantity for Octreotide API?
Mediocon Inc supplies Octreotide with a minimum order quantity of 1 kg (sample packs available for R&D). We accommodate both small R&D quantities and large commercial-scale orders. Contact our sales team at akshay@mediocon.com or +91 9309999757 for a tailored quote.
What pharmacopoeial grades of Octreotide does Mediocon supply?
We supply Octreotide conforming to IP / BP / EP / USP pharmacopoeial standards. Each batch is tested against full pharmacopoeial specifications and released with a Certificate of Analysis. Custom specifications can be accommodated for regulated markets.
What documentation is provided with Octreotide API?
Every shipment of Octreotide comes with: Certificate of Analysis (CoA), MSDS/SDS, Certificate of Origin (COO), and Drug Master File (DMF) support on request. We also provide GMP certification, ISO 9001:2015 compliance documentation, and full regulatory support for filings in USA (FDA), Europe (EMA), and other markets.
What is the lead time and shipping for Octreotide bulk orders?
Standard lead time for Octreotide is 2–4 weeks for standard orders; expedited shipments possible for urgent requirements. We ship to 40+ countries worldwide using approved pharmaceutical-grade packaging (25 kg HDPE drums / aluminium foil bags). All shipments include temperature-controlled logistics options where required by the product's storage conditions.
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