Octreotide Injection bulk supplier for pharma manufacturers

Octreotide Injection Suppliers & Bulk Manufacturers

Q: Does octreotide injection need refrigeration?

Ampoules and vials are normally stored at 2 to 8 Â°C and protected from light. Labels usually allow a short period at room temperature; follow the labelling of the product you buy.

Available Forms: Injection

Available Strengths: 50 mcg/mL, 100 mcg/mL, 200,cg/mL, 500 mcg/mL

Reference Brands: Sandostatin.(EU & US)

Category: Oncology Cancer Care

Octreotide Injection (50 mcg/mL, 100 mcg/mL, 200 mcg/mL, 500 mcg/mL) is used in oncology to manage symptoms and control growth in carcinoid tumors, gastroenteropancreatic neuroendocrine tumors (GEP-NETs), and acromegaly. Available in both U.S. and EU, this somatostatin analog is administered via subcutaneous or IV injection. It helps regulate hormone secretion, improving symptoms and tumor control in oncology patients, making it a key product in oncology B2B distribution.

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Product Description:

Octreotide is a synthetic peptide analogue of somatostatin. It suppresses growth hormone and several gut hormones, and is used for acromegaly and to control the flushing and diarrhoea caused by carcinoid tumours and VIP-secreting tumours; the long-acting form is also used to control some neuroendocrine tumours. The originator is Novartis's Sandostatin, an immediate-release injection given subcutaneously or intravenously, together with Sandostatin LAR, a monthly intramuscular depot of 10, 20 or 30 mg.

Sourcing octreotide injection

The immediate-release injection, in strengths from 50 to 1,000 mcg/mL, is made by many generic manufacturers, including in India. Long-acting depot versions are much harder to copy, because drug release depends on the microsphere manufacturing process; the first US generic of Sandostatin LAR was launched only in 2024. Ampoules and vials are normally stored at 2 to 8 °C; our cold chain explainer covers what importers should plan. We also list an octreotide acetate pen.

Octreotide API

Octreotide acetate API is made by peptide synthesis. When you source it, ask for a Certificate of Analysis to the USP or Ph. Eur. monograph covering assay, peptide-related impurities, acetate and water content and bacterial endotoxins, the site's GMP certificate, and a DMF or CEP where your market requires one. Our explainer on the Drug Master File covers the documents in more detail.

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Octreotide Injection — third party manufacturing & bulk supply

Octreotide Injection is available through PharmaTradz for wholesale and bulk supply as well as on a third party (contract) manufacturing basis. Buyers sourcing this product generally take one of three routes:

Wholesale / bulk supply Stock or scheduled supply from an existing manufacturer. The fastest route where the product is already registered in your market.

Third party manufacturing Manufactured to your specification and packed under your own brand and label — suits distributors and brand owners building a portfolio in their market.

Dossier licensing Where a CTD, EU-CTD or ACTD dossier exists it can often be licensed for filing in your name, compressing market entry from years to months.

Indicative minimum order quantity

Octreotide Injection is supplied as Injection — an injectable dosage form, so the indicative MOQ is 50,000 units. Actual MOQ is confirmed by the allocated manufacturer against your pack presentation and destination market. See full supply terms for dossier formats, market availability and shelf life.

Manufacturers of Octreotide Injection listed on PharmaTradz hold site-level approvals across WHO-GMP, EU-GMP, USFDA, ANVISA and TGA, verified at onboarding.

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Frequently Asked Questions

Acromegaly, and the flushing and diarrhoea caused by carcinoid tumours and VIP-secreting tumours. The long-acting form is also used to control some neuroendocrine tumours.

Sandostatin and Sandostatin LAR (Novartis) are the originator brands. Other products include Mycapssa oral capsules (US and EU), the Bynfezia pen (US), Oczyesa (EU) and many generic injections.

Ampoules and vials are normally stored at 2 to 8 °C and protected from light. Labels usually allow a short period at room temperature; follow the labelling of the product you buy.

Yes. Tell us the quantity and the documents your registration needs, and we will confirm availability, Certificate of Analysis, DMF or CEP status and lead time.