Comprehensive medication guide to Sandostatin including estimated pricing, availability information, side effects, and how to find it in stock at your local pharmacy.
Estimated Insurance Pricing
$0–$500/month specialty tier copay; Tier 4 on most Medicare Part D plans; prior authorization required by most plans; commercially insured patients may pay $0/month with the Novartis copay assistance card (up to $15,000/year coverage).
Estimated Cash Pricing
$40–$110 retail for generic immediate-release injection (10 vials); $3,000–$5,500/month for generic LAR (Teva); $6,700–$8,500/month for brand Sandostatin LAR Depot; as low as $41 with SingleCare or $89 with GoodRx for the immediate-release formulation.
Medfinder Findability Score
45/100
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Sandostatin is a brand name for octreotide acetate, a synthetic somatostatin analog manufactured by Novartis. It is a man-made version of somatostatin — a natural hormone produced by the hypothalamus, pancreas, and gastrointestinal tract that acts as the body's "off switch" for hormone secretion.
Sandostatin is FDA-approved for three conditions: acromegaly (excess growth hormone from a pituitary tumor), carcinoid syndrome (severe flushing and diarrhea from metastatic carcinoid tumors), and VIPomas (profuse watery diarrhea from VIP-secreting tumors). It is also widely used off-label for gastroenteropancreatic neuroendocrine tumors (GEP-NETs), esophageal variceal bleeding, hepatorenal syndrome, and dumping syndrome.
Sandostatin is available as an immediate-release injection (given multiple times daily) and as Sandostatin LAR Depot, a long-acting microsphere formulation given by intramuscular injection once every four weeks. Generic octreotide injection has been available for years; the first generic LAR formulation (Teva) was FDA-approved in October 2024. Mycapssa, the only oral octreotide, is approved for acromegaly maintenance only.
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Sandostatin (octreotide) is a synthetic octapeptide that mimics the active portion of natural somatostatin. It binds primarily to somatostatin receptor subtype 2 (SSTR2), which is the predominant somatostatin receptor on pituitary somatotroph cells and neuroendocrine tumor cells. Binding to SSTR2 activates intracellular signaling pathways that reduce cyclic AMP, decrease calcium entry into cells, and inhibit hormone-releasing vesicle secretion.
In acromegaly, this mechanism suppresses growth hormone (GH) and IGF-1 secretion from pituitary tumor cells, slowing or halting disease progression. In carcinoid syndrome and NETs, octreotide suppresses the secretion of serotonin, histamine, VIP, and other tumor-derived hormones that cause symptoms. It also has a mild antiproliferative effect in SSTR2-positive tumors.
Beyond its primary targets, octreotide suppresses insulin, glucagon, gastrin, TSH, and GI secretions — which explains both its broad therapeutic utility and its side effect profile including glucose dysregulation, hypothyroidism, and gallstone formation.
50 mcg/mL — injection
Immediate-release subcutaneous or IV injection
100 mcg/mL — injection
Immediate-release subcutaneous or IV injection
500 mcg/mL — injection
Immediate-release subcutaneous or IV injection
10 mg — injectable suspension
Sandostatin LAR Depot — IM gluteal injection every 4 weeks
20 mg — injectable suspension
Sandostatin LAR Depot — IM gluteal injection every 4 weeks (most common maintenance dose)
30 mg — injectable suspension
Sandostatin LAR Depot — IM gluteal injection every 4 weeks
Sandostatin has a findability score of 45 out of 100, indicating that it is frequently difficult to find — particularly in LAR (long-acting depot) formulations. As of 2025–2026, the immediate-release injection is available from multiple generic manufacturers (Avet, Fresenius Kabi, Hikma, Sagent), making it relatively accessible. However, the LAR formulations — which most long-term patients rely on — remain supply-constrained.
The shortage is driven by the extraordinary manufacturing complexity of the LAR microsphere formulation and a historically narrow supplier base. The FDA approved Teva's generic LAR in October 2024 and Viatris' generic in 2025, gradually expanding the manufacturer pool. However, supply inconsistency by region and formulation persists. Sandostatin LAR Depot is dispensed exclusively through specialty pharmacies, which further limits access compared to standard retail medications.
If you're having trouble filling your Sandostatin prescription, medfinder can contact pharmacies near you to find which ones have Sandostatin in stock — saving you hours of phone calls.
Sandostatin is not a controlled substance, so it can technically be prescribed by any licensed prescriber. However, most insurance plans require prior authorization with documentation from a specialist due to the high cost and specialty-only dispensing requirements. Common payer requirements specify prescribing by or in consultation with an endocrinologist, oncologist, or gastroenterologist.
Typical prescribers by indication:
Telehealth is limited for initial Sandostatin prescribing because diagnosis requires in-person testing (blood draws, imaging, GH/IGF-1 labs) and LAR injections must be given by a healthcare provider at a clinic. However, established patients with stable disease may use telehealth for follow-up visits, lab result reviews, dose adjustment discussions, and prescription refills.
No. Sandostatin (octreotide) is not a controlled substance and has no DEA schedule classification. It has no known abuse potential or dependency risk. Any licensed prescriber — including MDs, DOs, nurse practitioners, and physician assistants — can prescribe it without DEA authorization.
However, access to Sandostatin — particularly the LAR formulation — is tightly managed through other mechanisms: insurance prior authorization requirements (most plans require specialist prescribing and step therapy), specialty pharmacy dispensing requirements for the LAR formulation, and in some cases, prescriber specialty restrictions on certain insurance plans. These administrative controls mean that while Sandostatin is not legally restricted like a controlled substance, it is not easily obtained without specialist involvement.
The most frequently reported side effects are gastrointestinal, reflecting octreotide's suppression of GI hormones and motility:
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Lanreotide (Somatuline Depot)
First-generation somatostatin analog given as deep SC injection every 4 weeks via prefilled syringe. FDA-approved for acromegaly, GEP-NETs, and carcinoid syndrome. Manufactured by Ipsen on an independent supply chain — practical backup during Sandostatin shortages. Comparable clinical efficacy.
Pasireotide LAR (Signifor LAR)
Second-generation somatostatin analog binding SSTR1, 2, 3, and 5. Superior biochemical control for patients inadequately controlled on first-generation SSAs. Higher hyperglycemia risk requires additional glucose monitoring. Approved for acromegaly; not for carcinoid or VIPoma.
Mycapssa (oral octreotide)
Only FDA-approved oral octreotide. Delayed-release capsules for acromegaly maintenance in patients who have responded to injectable octreotide or lanreotide. Eliminates injections. Costs $8,000–$10,000/month. Not approved for carcinoid syndrome or VIPoma.
Pegvisomant (Somavert)
Growth hormone receptor antagonist with a different mechanism — blocks GH receptor binding rather than suppressing GH secretion. Used for acromegaly when SSAs provide inadequate control. Not effective for carcinoid or VIPoma.
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Lutetium Lu 177 dotatate (Lutathera)
majorOctreotide competitively binds somatostatin receptors, reducing PRRT efficacy. Must discontinue Sandostatin Injection at least 24 hours before each Lutathera dose. Patients on LAR must transition to short-acting octreotide.
Cyclosporine
majorOctreotide decreases cyclosporine blood levels, increasing risk of transplant rejection. Requires close cyclosporine monitoring and dose adjustment.
Insulin / antidiabetic agents
moderateOctreotide alters insulin-glucagon balance; blood glucose can swing high or low. Antidiabetic dose adjustment may be needed. Blood glucose monitoring required.
CYP3A4 substrates (quinidine, terfenadine)
moderateOctreotide may reduce clearance of CYP3A4-metabolized drugs via GH suppression. Narrow therapeutic index drugs should be monitored closely.
Bromocriptine
minorOctreotide may increase bromocriptine bioavailability. Generally minor but should be noted in patients on both drugs.
Sandostatin (octreotide) is a critical medication for patients with acromegaly, carcinoid syndrome, VIPomas, and neuroendocrine tumors. It is highly effective at controlling the hormonal excess that drives these conditions, significantly improving quality of life and, in some cases, slowing disease progression. However, it is one of the more challenging specialty medications to access — requiring specialist prescribing, specialty pharmacy dispensing, insurance prior authorization, and careful monitoring.
Cost is a significant concern, but multiple assistance pathways exist. Commercially insured patients should enroll in the Novartis copay card (up to $15,000/year), which can reduce out-of-pocket costs to $0. Uninsured or underinsured patients should apply for the Novartis Patient Assistance Foundation. Generic octreotide LAR (Teva and Viatris) now provides a more affordable alternative for patients without robust copay support.
Supply remains inconsistent in 2026, particularly for the LAR formulation. If you're struggling to find Sandostatin in stock, medfinder can help locate pharmacies with current availability near you — saving you hours of phone calls and getting you back on your treatment faster.
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