Octreotide
Octreotide is a synthetic hormone-like medicine used to treat acromegaly (a condition of excess growth hormone) and to control severe diarrhea and flushing caused by certain hormone-secreting tumors.
🧬 Where this information comes from Click to expand
The clinical label records used on this page are FDA-filed Structured Product Labeling (SPL) retrieved through openFDA. We identified 14 clinical label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. Forms, routes, brands, labelers, strengths, and NDC product-record counts are built separately from matching FDA National Drug Code Directory records. The linked DailyMed document is a representative official source for verification, not the page’s only clinical source. View the linked label on DailyMed →
📖 Octreotide: Patient Information Guide
A plain-language walkthrough of Octreotide — what it treats, how it works, how it’s taken, side effects, warnings and interactions. Tap any section to expand it.
🎯What it's used for▾
Octreotide is a somatostatin analogue (a synthetic copy of a natural hormone) approved across several products and formulations for the following conditions:
- Acromegaly — All octreotide injection products (Sandostatin, BYNFEZIA Pen, and octreotide acetate injections) are approved to lower growth hormone (GH) and IGF-1 levels in patients who have not responded adequately to surgery, radiation, or bromocriptine. Mycapssa (oral capsule) is approved specifically for long-term maintenance in acromegaly patients who have already responded to and tolerated octreotide or lanreotide injections.
- Metastatic carcinoid tumors — Octreotide acetate injections and Sandostatin injection are approved to reduce the severe diarrhea and flushing episodes these tumors cause. Note: clinical trials with injection formulations did not demonstrate shrinkage of tumors or slowing of tumor growth.
- VIPomas (vasoactive intestinal peptide-secreting tumors) — Octreotide acetate injections, BYNFEZIA Pen, and Sandostatin injection are approved for the profuse watery diarrhea caused by these tumors. The same limitation regarding tumor size and growth applies.
⚙️How it works▾
Octreotide works by mimicking somatostatin, a hormone your body naturally produces to put the brakes on other hormones. It is a far more potent version of somatostatin — blocking the release of growth hormone, glucagon, insulin, serotonin, VIP, and several other gut hormones. In acromegaly, this brings dangerously high growth hormone levels down. In carcinoid tumors and VIPomas, it quiets the flood of hormones those tumors release, which is what causes the debilitating diarrhea and flushing episodes.
💊How it's taken▾
Octreotide is available as injections (given under the skin or into a vein) and as Mycapssa, an oral delayed-release capsule. Injection products are typically given multiple times per day; injection sites should be rotated regularly to avoid irritation. Mycapssa is taken by mouth twice daily on a completely empty stomach — food reduces absorption by roughly 90%, so timing really matters. Your prescriber will adjust your dose based on your hormone levels and symptoms over time. Always follow your personalized prescription instructions.
🤒Side effects — in detail▾
The most common side effects of octreotide include:
- Diarrhea and loose stools
- Abdominal pain or cramping
- Nausea and vomiting
- Gas and bloating
- Headache
- Dizziness and fatigue
- Injection site pain (with injectable forms)
- Constipation
More serious reactions — including gallstone complications, heart rhythm changes, significant blood sugar swings, and hypothyroidism — require prompt medical attention. Contact your doctor right away if you develop severe stomach pain, yellowing of the skin, a very slow or irregular heartbeat, or signs of dangerously low blood sugar.
⚠️Warnings & precautions▾
- Gallstones and gallbladder problems: Octreotide slows gallbladder emptying, and over half of long-term users develop some gallbladder abnormality. Serious complications like acute cholecystitis, bile duct blockage, or pancreatitis can occur and may require stopping treatment.
- Heart rhythm problems: Octreotide can slow the heart rate, cause conduction abnormalities, and — especially when given intravenously at high doses — has been linked to complete heart block. Cardiac monitoring is recommended for IV use.
- Blood sugar changes: By altering the balance of insulin and glucagon, octreotide can cause both low blood sugar (hypoglycemia) and high blood sugar (hyperglycemia). Diabetic patients need especially close monitoring.
- Hypothyroidism: Octreotide suppresses the thyroid-stimulating hormone and can cause an underactive thyroid over time. Thyroid function should be checked periodically during long-term use.
- Fat malabsorption: Octreotide can reduce pancreatic enzyme output, leading to greasy stools, bloating, and weight loss. Report these symptoms to your doctor.
- Vitamin B12: Some patients develop lower vitamin B12 levels during treatment; periodic monitoring is recommended.
🔀What it interacts with▾
Octreotide can interact with a number of medications — tell your doctor and pharmacist everything you take:
- Antacids, PPIs, and H2-blockers (e.g., omeprazole, famotidine): reduce Mycapssa absorption — a higher dose of Mycapssa may be needed
- Insulin and diabetes medicines: octreotide changes blood sugar balance, so doses of these drugs may need adjustment
- Cyclosporine: Mycapssa can lower cyclosporine levels, possibly reducing its effectiveness
- Digoxin: Mycapssa may reduce digoxin levels — careful monitoring needed given digoxin's narrow safety margin
- Lisinopril: Mycapssa may increase lisinopril levels, raising the risk of low blood pressure
- Hormonal birth control containing levonorgestrel: Mycapssa may reduce its effectiveness — use a backup contraceptive method
- Bromocriptine: octreotide may increase bromocriptine exposure — dose adjustment may be needed
- Beta-blockers and calcium channel blockers: octreotide's heart-rate-slowing effect can compound theirs — dose adjustments may be needed
- CYP3A4-metabolized drugs with a narrow safety window (e.g., quinidine): octreotide may increase their levels — use with extra caution and monitoring
This is not a complete list of interactions. Always talk with your doctor or pharmacist before starting, stopping, or changing any medication.
📋Before taking it▾
- Allergy to octreotide: Do not take if you have had a severe allergic reaction (including anaphylaxis) to octreotide or any component of the product
- Heart problems: Tell your doctor if you have a slow heart rate, heart rhythm disorder, or heart failure — octreotide can worsen these
- Gallbladder disease: Tell your doctor about any history of gallstones — your risk of new or worsening gallbladder problems is increased
- Diabetes or blood sugar disorders: Glucose monitoring is essential; your diabetes medicines may need dose changes
- Thyroid disease: Octreotide can suppress thyroid function — baseline and periodic thyroid tests are recommended
- Kidney failure requiring dialysis: Drug exposure is higher — lower starting doses are recommended
- Liver cirrhosis: Drug is cleared more slowly — lower starting doses are recommended
- Pregnancy: Data are limited; discuss risks with your doctor. Women with acromegaly should know that normalizing IGF-1 may improve fertility — use effective contraception if pregnancy is not desired
- Breastfeeding: It is not known whether octreotide passes into human breast milk — weigh the benefits and risks with your doctor
- Children: Safety and efficacy of injectable suspension have not been established in children under 6; serious adverse events including death have been reported in children under 2 with octreotide acetate injection
- Older adults: The drug is cleared more slowly in people 65 and older — careful, cautious dosing is recommended
🚑If you take too much▾
Too much octreotide can cause serious heart problems (including arrhythmia and complete heart block), very low blood pressure, pancreatitis, liver inflammation, lactic acidosis, diarrhea, flushing, and extreme fatigue. If you suspect an overdose, treatment is focused on managing symptoms. Contact the National Poison Control Center at 1-800-222-1222 or seek emergency medical care immediately.
📡Pharmacodynamics — effects in the body▾
Octreotide measurably lowers growth hormone and IGF-1 levels in patients with acromegaly and can normalize them in many cases. It also reduces gallbladder contractions and bile flow, which is why gallstone formation is a known risk with long-term use. Octreotide can meaningfully suppress TSH (thyroid-stimulating hormone), potentially causing an underactive thyroid. When taken as Mycapssa, it temporarily increases intestinal permeability to allow absorption — an effect that is fully reversed within about 5.5 hours.
🔬Pharmacokinetics — how your body processes it▾
When injected subcutaneously, octreotide is absorbed rapidly, reaching peak blood levels within about 0.4 hours. It is about 65% bound to proteins in the blood, primarily lipoproteins. The drug has a short elimination half-life of roughly 1.7–2.7 hours after injection, though it acts longer than that in practice. About 32% is excreted unchanged in the urine. Elimination is significantly slower in people with liver cirrhosis or severe kidney failure requiring dialysis, and also slows with age — all of which can mean higher drug exposure and a need for lower doses. Mycapssa, the oral form, must be taken on an empty stomach because food reduces its absorption by about 90%.
📦How to store it▾
Store refrigerated between 2° and 8°C (36° and 46°F). Protect from light.
📄 Written from Octreotide’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Every point is grounded in that labeling — nothing is invented. How we use AI →
Supplements & herbs that interact with Octreotide
30 supplements and herbal products have documented interactions with Octreotide in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 1
- Moderate · 19
- Minor · 10
Educational information from a licensed clinical database (Natural Medicines) — see our data sources & update cadence. Not medical advice: an interaction being documented does not mean it will happen to you; do not start or stop medications or supplements without professional guidance.
🩺 Pharmacist Counseling Corner
Quick, plain-English answers to the questions patients ask most about Octreotide — the kind of thing our pharmacy team would talk through with you at the counter.
What exactly does octreotide do — and why do I need it? ▾
How do I take Mycapssa correctly — does it matter if I eat first? ▾
What side effects should I expect, and which ones mean I need to call my doctor? ▾
I've heard octreotide can cause gallstones. How serious is that risk? ▾
Can octreotide affect my blood sugar or other lab values? ▾
I'm a woman of childbearing age — is there anything I should know about octreotide and pregnancy or birth control? ▾
Is Octreotide available over the counter? ▾
When was Octreotide first available? ▾
Who makes Octreotide? ▾
💬 Answers drafted from Octreotide’s FDA-approved label information, summarized in plain language with AI, and reviewed by our pharmacy team before publication. Grounded in that labeling — nothing is made up. How we use AI →
🧰 Keep exploring
💊 How Octreotide comes
Octreotide is available in 2 forms. Different forms and brands can have different approved uses, doses, schedules, and directions. Follow the instructions for your exact product, and do not switch forms without guidance from your prescriber or pharmacist.
Injection
How this form is used
- Octreotide acetate injection and Sandostatin injection are used to reduce growth hormone and IGF-1 levels in acromegaly when surgery, radiation, or other treatments have not worked well enough
- BYNFEZIA Pen is used to reduce growth hormone and IGF-1 levels in acromegaly
- Octreotide acetate injection and Sandostatin are used to treat severe diarrhea and flushing episodes from metastatic carcinoid tumors
- Octreotide acetate injection, BYNFEZIA Pen, and Sandostatin are used to treat profuse watery diarrhea caused by VIPomas
- BYNFEZIA Pen is given only by subcutaneous (under-the-skin) injection; rotate injection sites among the abdomen, front of the thighs, or back of the upper arms
- Sandostatin injection and octreotide acetate injection may be given subcutaneously or intravenously; rotate subcutaneous injection sites regularly
- BYNFEZIA Pen should be at room temperature before injecting to reduce injection-site reactions
- Octreotide acetate injection and Sandostatin injection are given multiple times daily as directed by your prescriber — follow the schedule exactly
Delayed-release capsule
How this form is used
- Mycapssa is approved for long-term maintenance treatment of acromegaly in patients who have already responded to and tolerated octreotide or lanreotide injections
- Mycapssa must be taken on an empty stomach — at least 1 hour before a meal or at least 2 hours after eating
- Mycapssa should be swallowed with a full glass of water
- Taking Mycapssa with food can reduce absorption by approximately 90% — do not take it with meals
- IGF-1 levels and symptoms should be monitored every two weeks during dose adjustment, then monthly once a stable dose is reached
📊 Octreotide across the U.S. market
How Octreotide appears in the FDA’s National Drug Code Directory — including its dosage forms, strengths, brand names, manufacturers, and FDA-listed product records. These are directory records, not sales or prescription volume.
FDA-listed product records by dose form (tablet variants merged) — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
Also listed with the FDA, not a patient dose form: Powder (20) · Kit (18) — bulk drug substance sold to compounders/manufacturers and multi-item kits. These aren’t counted in the dose-form total above.
Share of FDA-listed product records by manufacturer — FDA National Drug Code Directory. Record counts are not sales or prescription volume.
📈 How widely Octreotide is used
A general measure of how commonly Octreotide is prescribed, based on Medicaid — one of the largest public drug programs. The figure below is prescriptions filled in Q1–Q4 2025, summed across every form and brand of the drug.
Think of this as a proxy for how widely Octreotide is used, drawn from freely available public data. Medicaid is just one program — these numbers don’t include Medicare, other government coverage, or commercial and cash-pay prescriptions, so real-world use is higher than what’s shown here.
How commonly is Octreotide prescribed? Of the 1,596 medications we measure, Octreotide ranks #993 by Medicaid prescriptions — more than 38% of them.
Utilization by Octreotide product
Pick a product to see its own Medicaid numbers. Each chip is one clinical product — a specific strength & dosage form as defined by RxNorm — with brand-name and generic versions combined.
octreotide 30 MG Injection Most dispensed
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 898601
octreotide 20 MG Injection
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 898589
1 ML octreotide 0.1 MG/ML Injection
Summed across the 6 of 25 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 312069
octreotide 0.2 MG/ML Injectable Solution
Summed across the 2 of 8 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 314152
1 ML octreotide 0.5 MG/ML Injection
Summed across the 3 of 22 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 312070
octreotide 1 MG/ML Injectable Solution
Summed across the 3 of 8 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 312071
octreotide 20 MG Delayed Release Oral Capsule
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2380611
1 ML octreotide 0.05 MG/ML Prefilled Syringe
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1090559
1 ML octreotide 0.05 MG/ML Injection
Summed across the 2 of 17 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 312068
1 ML octreotide 0.1 MG/ML Prefilled Syringe
Summed across the 1 of 2 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1090558
octreotide 10 MG Injection
Summed across the 1 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 898605
Shares are of the Medicaid prescriptions shown here. Product grouping follows RxNorm (the National Library of Medicine’s drug terminology), so “one product” means one strength & dosage form regardless of manufacturer. Dollar figures are gross Medicaid reimbursement before mandatory rebates — rebates (often large, especially for brand-name drugs) are confidential, so actual net cost to Medicaid is lower than shown.
Source: Medicaid State Drug Utilization Data (CMS), aggregated by generic ingredient — summed across every NDC (all brands, strengths, salt forms and dosage forms) of Octreotide, and across all states and both fee-for-service and managed-care claims. A general popularity signal; it excludes Medicare, commercial insurance and cash prescriptions, so it is not total U.S. use. Based on the 24 of 104 listed Octreotide NDCs with Medicaid activity.
🔍 Compare Octreotide products
A representative set of FDA-listed product records for Octreotide — across manufacturers, strengths, and dosage forms, grouped by form with each product’s manufacturer and how the FDA approved it. The same medicine may be made and packaged by different companies, so a single drug can have many directory entries. (It’s also why a refill can look different — a new shape, color, or box — even though it contains the same medication.)
| Strength | Route | Manufacturer / Labeler | Category ⓘ | Details |
|---|---|---|---|---|
| 💊Delayed-release capsule | ||||
| 20 mg | Oral | Amryt Pharmaceuticals Designated Activity Company × 2 listings | NDA | View NDC → |
| 20 mg | Oral | Chiasma Inc. | NDA | View NDC → |
| 20 mg | Oral | Chiesi USA, Inc. | NDA | View NDC → |
| 💊Injection | ||||
| 100 mcg/mL | Intravenous; Subcutaneous | Bryant Ranch Prepack | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Fresenius Kabi USA, LLC × 2 listings | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Fresenius Kabi USA, LLC × 2 listings | ANDA | View NDC → |
| 200 mcg/mL | Intravenous, Subcutaneous | Fresenius Kabi USA, LLC | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Fresenius Kabi USA, LLC | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Fresenius Kabi USA, LLC × 2 listings | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Fresenius Kabi USA, LLC × 2 listings | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous, Subcutaneous | Fresenius Kabi USA, LLC | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Fresenius Kabi USA, LLC | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 200 mcg/mL | Intravenous, Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous, Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Gland Pharma Limited | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Glenmark Pharmaceuticals Inc., Usa | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Glenmark Pharmaceuticals Inc., Usa | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Glenmark Pharmaceuticals Inc., Usa | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Glenmark Pharmaceuticals Inc., Usa | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Hainan Shuangcheng Pharmaceuticals Co., Ltd. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 200 mcg/mL | Intravenous, Intravenous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous, Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 200 mcg/mL | Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous, Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Meitheal Pharmaceuticals, Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Meitheal Pharmaceuticals, Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Meitheal Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Mylan Institutional LLC | ANDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Mylan Institutional LLC × 2 listings | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Mylan Institutional LLC | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Mylan Institutional LLC × 2 listings | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Mylan Institutional LLC | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Mylan Institutional LLC × 2 listings | ANDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Novartis Pharmaceuticals Corporation × 2 listings | NDA | View NDC → |
| 50 mcg/mL | Intravenous, Subcutaneous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Sagent Pharmaceuticals × 2 listings | ANDA | View NDC → |
| 100 mcg/mL | Intravenous, Subcutaneous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Sagent Pharmaceuticals × 2 listings | ANDA | View NDC → |
| 200 mcg/mL | Intravenous, Subcutaneous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Sagent Pharmaceuticals × 2 listings | ANDA | View NDC → |
| 500 mcg/mL | Intravenous, Subcutaneous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Sagent Pharmaceuticals × 2 listings | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous, Subcutaneous | Sagent Pharmaceuticals | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Sagent Pharmaceuticals × 2 listings | ANDA | View NDC → |
| 2.5 mg/mL | Subcutaneous | Sun Pharmaceutical Industries, Inc. | NDA | View NDC → |
| 50 mcg/mL | Intravenous; Subcutaneous | Teva Parenteral Medicines, Inc. | ANDA | View NDC → |
| 100 mcg/mL | Intravenous; Subcutaneous | Teva Parenteral Medicines, Inc. | ANDA | View NDC → |
| 200 mcg/mL | Intravenous; Subcutaneous | Teva Parenteral Medicines, Inc. | ANDA | View NDC → |
| 500 mcg/mL | Intravenous; Subcutaneous | Teva Parenteral Medicines, Inc. | ANDA | View NDC → |
| 1000 mcg/mL | Intravenous; Subcutaneous | Teva Parenteral Medicines, Inc. | ANDA | View NDC → |
| 💊Kits | ||||
| — | — | Mylan Institutional LLC × 6 listings | ANDA | View NDC → |
| — | — | Novartis Pharmaceuticals Corporation × 9 listings | NDA | View NDC → |
| — | Intramuscular | Teva Pharmaceuticals, Inc. × 3 listings | ANDA | View NDC → |
| 💊Bulk drug substance | ||||
| 1 g/g | — | Ambiopharm, Inc. | BULK INGREDIENT | View NDC → |
| 100 kg/100 kg | — | Assia Chemical Industries Ltd - Teva Tech Site | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Aurobindo Pharma Limited | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Bachem AG × 2 listings | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Bachem Americas, Inc. | BULK INGREDIENT FOR HUMAN PRESCRIPTION COMPOUNDING | View NDC → |
| 1 g/g | — | Bachem Americas, Inc. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Bcn Peptides Sa | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Chemical & Biopharmaceutical Laboratories of Patras Single Member S.A. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Chengdu Shengnuo Biopharm Co. Ltd. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Fresenius Kabi Ipsum Srl | BULK INGREDIENT | View NDC → |
| 500 g/500 g | — | Hainan Shuangcheng Pharmaceuticals Co., Ltd. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | LSNE, Inc. | BULK INGREDIENT | View NDC → |
| 1 kg/kg | — | Matrix Pharmacorp Private Limited | BULK INGREDIENT | View NDC → |
| 6 g/6 g | — | PolyPeptide Laboratories, Pvt. Ltd. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | ScinoPharm Taiwan Ltd. | BULK INGREDIENT | View NDC → |
| 1 g/g | — | Sinopep-Allsino Biopharmaceutical Co., Ltd. | BULK INGREDIENT | View NDC → |
| 3 kg/3 kg | — | Sterling Pharma Solutions Limited | BULK INGREDIENT | View NDC → |
| 24 kg/24 kg | — | Sun Pharmaceutical Industries, Inc. | BULK INGREDIENT | View NDC → |
| 100 g/100 g | — | USV Private Limited | BULK INGREDIENT | View NDC → |
Showing 133 of 133 products — FDA National Drug Code Directory. See every product, package size and price: browse all 133 Octreotide NDCs →
📈 What people report — real-world data (FDA FAERS)
After a medicine reaches the market, patients, doctors and drugmakers can send the FDA reports of problems they think may be linked to it. Here’s what’s been reported for Octreotide — a signal of what to watch for, not proof the drug caused it.
Source: openFDA, from the FDA Adverse Event Reporting System (FAERS). These are voluntary reports — they don’t prove the drug caused the effect, and counts reflect how often something was reported, not how often it actually happens. Reports also often name the very problem the medicine is taken for — a common reason to file one is that the drug didn’t help — so for a pain reliever you may see “pain” high on the list; that points to why the report was filed, not to the drug causing the symptom. This counts every report that lists Octreotide in any role, so the total runs higher than the FDA’s official dashboard, which counts only cases where the drug is the suspect. For the authoritative figures, see the FDA FAERS Public Dashboard. Always talk to your pharmacist or doctor.
🏛️ The road to your pharmacy
How Octreotide went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
🚨 Recall history
A recall is when a specific batch of a medicine is pulled from the market — usually a manufacturing issue, not a problem with the drug itself. Class I is most serious, Class III least.
Source: openFDA drug enforcement (recall) reports.
RxNorm Concept Web — From Ingredient to Every Form and Strength
This page starts with one ingredient concept (IN). The branches below show its dose-form concepts (SCDF), then the available clinical drug and strength concepts (SCD). Combination products remain separate concepts with their own pages.
RxCUI 7617 5 dose forms · 13 strengths
-
Dose form (SCDF) Delayed Release Oral Capsule RxCUI 2380610In current FDA listingsClinical drug / strength (SCD) 20 MGRxCUI 2380611 -
Dose form (SCDF) Injectable Solution RxCUI 373140In current FDA listings -
Dose form (SCDF) Injection RxCUI 1654342In current FDA listingsClinical drug / strength (SCD) 1 ML octreotide 0.05 MG/MLRxCUI 3120681 ML octreotide 0.1 MG/MLRxCUI 3120691 ML octreotide 0.5 MG/MLRxCUI 31207010 MGRxCUI 89860520 MGRxCUI 89858930 MGRxCUI 898601 -
Dose form (SCDF) Pen Injector RxCUI 2360542In current FDA listingsClinical drug / strength (SCD) 2.8 ML octreotide 2.5 MG/MLRxCUI 2360543 -
Dose form (SCDF) Prefilled Syringe RxCUI 1090557No current FDA listingClinical drug / strength (SCD) 1 ML octreotide 0.05 MG/MLRxCUI 10905591 ML octreotide 0.1 MG/MLRxCUI 10905581 ML octreotide 0.5 MG/MLRxCUI 1090560
Look up RxCUI 7617 in the RxCUI Atlas →
RxNorm is the U.S. National Library of Medicine’s normalized drug vocabulary. Its concept hierarchy can include forms that are not currently marketed; the status on each branch compares that concept with current FDA listings. RxCUIs identify vocabulary concepts, not individual packages or manufacturers.
📦 Supply & shortage status
Whether Octreotide is in short supply in the U.S. right now, plus any shortage history the FDA has on record. A shortage usually reflects a manufacturing or demand issue — not a safety problem with the drug.
Source: openFDA, from the FDA Drug Shortages database.
🏷️ Sold under these brand names
🏭 Manufacturers & labelers
…and 9 more on the FDA NDC directory.
RxNorm drug class
Octreotide belongs to the Somatostatin Analog class.
Classified by RxNorm RxClass — the U.S. National Library of Medicine's standardized drug-classification service (Established Pharmacologic Class from the FDA, the ATC drug family from the WHO, and mechanism of action). Reference only, not medical advice.
🔬 Where this comes from
Core label, product, RxNorm, safety, and utilization data on this page come from the sources identified below. AI-written, editorial, and licensed sections are labeled separately.
How we combine label and product data
HelloPharmacist combines public FDA and NLM records; we don’t author the underlying clinical facts. We identified 14 FDA-filed SPL label sets within the page’s selected clinical scope after exact ingredient or ingredient-combination matching and applicable route/form matching. The representative label is the starting point for the displayed reference monograph; the 12 largest stored in-scope SPL records, which may include that representative, are compared section by section, and the longest available version of each section is retained. Forms, routes, brands, labelers, product-listed strengths, and product-record counts are aggregated separately from ingredient-matched FDA NDC Directory records; package records listed above are associated with the linked SPL; and the normalized concept hierarchy comes from NLM RxNorm.
For canonical ingredient pages, bounded product-attributed indication and administration excerpts may be added to the AI evidence, and the generator is instructed to preserve available product, brand, route, and form qualifiers instead of treating one label as universal. Where a section is identified as AI-written, its plain-language text is generated from bounded label evidence. New draft drug pages remain in the admin review queue before first publication. Teva Pharmaceuticals, Inc. is the representative DailyMed label linked for verification and dates; it is not the sole source used for the page.
This is general education, not medical advice — always consult your doctor or pharmacist about your medications and any medical condition. For the exact wording of the linked representative label, view that label on DailyMed; some displayed composite sections may come from other in-scope SPL labels. Learn how we use AI and our data sources & update cadence.