Eltrombopag
Eltrombopag is a platelet-boosting medicine (a thrombopoietin receptor agonist) used for low platelet counts from immune thrombocytopenia (ITP) or chronic hepatitis C, and for severe aplastic anemia.
🧬 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 16 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 →
Eltrombopag (Promacta, Alvaiz) is a specialist medicine that raises low platelet counts by mimicking thrombopoietin, the body's natural platelet-growth signal. It is used for immune thrombocytopenia (ITP) after other treatments fall short, for low platelets from chronic hepatitis C, and for severe aplastic anemia, and it has been around since about 2008 and is available generically. It is usually fairly well tolerated, with nausea, diarrhea, headache and tiredness the complaints people notice most. The one thing to watch is its boxed warning for serious, even life-threatening liver damage (and worsening liver function in hepatitis C when paired with interferon and ribavirin), so regular liver blood tests are essential.
Clinical pearls
- Keep it at least 2 hours before or 4 hours after dairy, antacids and mineral supplements like iron, calcium or zinc.
- If you take a statin, especially rosuvastatin, your prescriber may lower its dose because eltrombopag can push statin levels up.
- Tell the lab you take eltrombopag, since it can interfere with some bilirubin and creatinine test results.
- Get an eye exam before starting and report any vision changes, because cataracts can develop or worsen on eltrombopag.
⚠️ FDA Boxed Warning — the FDA’s strongest safety alert ▾
Eltrombopag can cause serious, even life-threatening liver damage. If you have chronic hepatitis C and take it with interferon and ribavirin, it may also raise the risk of your liver function worsening (hepatic decompensation).
Your doctor will check liver blood tests before you start and regularly during treatment. Watch for yellow skin or eyes, dark urine, belly swelling, or confusion, and call your doctor right away if they appear.
Patient information guide A plain-language walkthrough of Eltrombopag, written from its FDA label.
What Eltrombopag is used for
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Eltrombopag treats low platelet counts and a bone marrow failure condition. Uses by product:
- Persistent or chronic ITP: eltrombopag tablets, eltrombopag for oral suspension, and Promacta are used in patients 1 year and older who did not respond enough to corticosteroids, immunoglobulins, or splenectomy. Alvaiz is used in patients 6 years and older.
- Chronic hepatitis C: treats low platelets so interferon-based therapy can start and continue. Alvaiz is for adults.
- Severe aplastic anemia, first-line: eltrombopag tablets and Promacta, with standard immunosuppressive therapy, in patients 2 years and older.
- Severe aplastic anemia, after insufficient response to immunosuppressive therapy: eltrombopag tablets, eltrombopag for oral suspension, and Promacta. Alvaiz is for adults.
It is not for myelodysplastic syndrome (MDS).
How Eltrombopag works
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Eltrombopag is a thrombopoietin (TPO) receptor agonist. It binds the TPO receptor (cMpl) and starts signals that make platelet-producing cells multiply and mature. That leads to more platelets.
Eltrombopag dosage
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Eltrombopag is taken by mouth, usually once daily, as tablets or an oral suspension depending on the product.
- Take it on an empty stomach or with a low-calcium meal.
- Separate it from antacids, dairy, and mineral supplements by 2 hours before or 4 hours after.
- Your prescriber adjusts the amount based on platelet counts and other factors.
- Alvaiz cannot be swapped milligram-for-milligram with other eltrombopag products.
Dosing details from the FDA-approved label
From the Eltrombopag prescribing information (“Dosage and Administration”). Doses are set by your prescriber for your product, condition, kidney function and age — never change a dose on your own.
- Persistent or Chronic ITP (adult and pediatric patients 6 years and older)
- 50 mg orally once daily
- 25 mg orally once daily for patients of East-/Southeast-Asian ancestry or with mild, moderate, or severe hepatic impairment (Child-Pugh class A, B, C)
- Consider 12.5 mg orally once daily for patients of East-/Southeast-Asian ancestry with hepatic impairment
- Maximum: Do not exceed 75 mg per day
- Adjust to maintain platelet count greater than or equal to 50 x 10^9/L; take without a meal or with a meal low in calcium (≤ 50 mg)
- Persistent or Chronic ITP (pediatric patients aged 1 to 5 years)
- 25 mg orally once daily
- Maximum: Do not exceed 75 mg per day
- Adjust to maintain platelet count greater than or equal to 50 x 10^9/L
- Chronic Hepatitis C-associated Thrombocytopenia
- Initiate at 25 mg orally once daily for all patients
- Adjust to achieve target platelet count required to initiate antiviral therapy
- Maximum: Do not exceed a daily dose of 100 mg
- First-line Severe Aplastic Anemia
- Orally once daily at 2.5 mg/kg (pediatric patients aged 2 to 5 years), 75 mg (pediatric patients aged 6 to 11 years) or 150 mg (patients aged 12 years and older) concurrently with standard immunosuppressive therapy
- Reduce initial dose in patients of East-/Southeast-Asian ancestry; modify dosage for toxicity or elevated platelet counts
- Refractory Severe Aplastic Anemia
- Initiate at 50 mg orally once daily
- Maximum: Do not exceed 150 mg per day
- Reduce initial dose in patients with hepatic impairment or of East-/Southeast-Asian ancestry; adjust to maintain platelet count greater than 50 x 10^9/L
- Alvaiz - Persistent or Chronic ITP (adult and pediatric patients 6 years and older)
- 36 mg orally once daily
- 18 mg orally once daily for patients of East-/Southeast-Asian ancestry or with mild to severe hepatic impairment
- Maximum: Do not exceed 54 mg per day
- Alvaiz is not substitutable with other eltrombopag products on a milligram per milligram basis
- Alvaiz - Chronic Hepatitis C-associated Thrombocytopenia
- Initiate at 18 mg orally once daily for all patients
- Adjust to achieve target platelet count required to initiate antiviral therapy
- Maximum: Do not exceed a daily dose of 72 mg
- Not substitutable with other eltrombopag products on a milligram per milligram basis
- Alvaiz - Refractory Severe Aplastic Anemia
- Initiate at 36 mg orally once daily
- Maximum: Do not exceed 108 mg per day
- Reduce initial dose in patients with hepatic impairment or of East-/Southeast-Asian ancestry
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Take eltrombopag tablets without a meal or with a meal low in calcium (≤ 50 mg). Take eltrombopag tablets at least 2 hours before or 4 hours after any medications or products containing polyvalent cations, such as antacids, calcium-rich foods, and mineral supplements. (2.4, 7.1, 12.3) Persistent or Chronic ITP:Initiate eltrombopag tablets at 50 mg orally once daily for most adult and pediatric patients 6 years and older, and at 25 mg orally once daily for pediatric patients aged 1 to 5 years. Dose reductions are needed for patients with hepatic impairment and some patients of East-/Southeast-Asian ancestry. Adjust to maintain platelet count greater than or equal to 50 x 10 9/L. Do not exceed 75 mg per day. (2.1, 8.6, 8.7) Chronic Hepatitis C-associated Thrombocytopenia:Initiate eltrombopag tablets at 25 mg orally once daily for all patients. Adjust to achieve target platelet count required to initiate antiviral therapy. Do not exceed a daily dose of 100 mg. (2.2) First-line Severe Aplastic Anemia:Initiate eltrombopag tablets orally once daily at 2.5 mg/kg (in pediatric patients aged 2 to 5 years old), 75 mg (pediatric patients aged 6 to 11 years old), or 150 mg for patients aged 12 years and older concurrently with standard immunosuppressive therapy. Reduce initial dose in patients of East-/Southeast-Asian ancestry. Modify dosage for toxicity or elevated platelet counts. (2.3, 8.7) Refractory Severe Aplastic Anemia:Initiate eltrombopag tablets orally at 50 mg once daily. Reduce initial dose in patients with hepatic impairment or patients of East-/Southeast-Asian ancestry. Adjust to maintain platelet count greater than 50 x 10 9/L. Do not exceed 150 mg per day. (2.3, 8.6, 8.7) 2.1 Persistent or Chronic Immune Thrombocytopenia Use the lowest dose of eltrombopag tablets to achieve and maintain a platelet count greater than or equal to 50 x 10 9 /L as necessary to reduce the risk for bleeding. Dose adjustments are based upon the platelet count response. Do not use eltrombopag tablets to normalize platelet counts [see Warnings and Precautions (5.4)]. In clinical trials, platelet counts generally increased within 1 to 2 weeks after starting eltrombopag tablets and decreased within 1 to 2 weeks after discontinuing eltrombopag tablets [see Clinical Studies (14.1)] .
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Eltrombopag side effects
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Common side effects vary by condition and include:
Common side effects
- Nausea
- Diarrhea
- Headache
- Fatigue
- Fever
- Cough
- Anemia (low red blood cells)
- Raised liver blood tests (ALT/AST)
- Cough and upper respiratory infections
When to get medical help
- Yellowing of your skin or eyes, dark urine, or severe belly pain: these can signal liver injury.
- Swelling or fluid in the belly or confusion, especially if you have hepatitis C: these can signal liver decompensation.
- Belly pain with nausea, vomiting, or diarrhea: this can signal a blood clot in a liver vein (portal vein thrombosis).
- Signs of a blood clot, such as sudden leg swelling or pain, chest pain, or shortness of breath.
- Changes in vision, since cataracts can develop or worsen.
- Unusual bleeding or bruising.
Eltrombopag warnings and precautions
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- Liver damage (boxed warning): can be severe and life-threatening. Liver tests are checked before and during treatment.
- Hepatitis C: with interferon and ribavirin, risk of liver decompensation rises, especially with low albumin or higher MELD scores.
- Blood clots: including portal vein clots in chronic liver disease. Do not aim to normalize platelet counts.
- MDS: higher risk of death and progression to acute myeloid leukemia in a trial.
- Cataracts: eye exams before and during treatment.
- Lab test interference: eltrombopag can distort bilirubin and creatinine results.
Eltrombopag interactions
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These can change how eltrombopag or other medicines work:
- Antacids, dairy, calcium-rich foods, mineral supplements: bind eltrombopag and reduce absorption.
- Statins (such as rosuvastatin) and other OATP1B1/BCRP drugs: levels may rise, so doses may need reducing.
- Interferon plus ribavirin: raises liver decompensation risk in hepatitis C.
- Lab tests: eltrombopag is highly colored and can interfere with results.
Interactions listed in the FDA-approved label
From the Eltrombopag prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Polyvalent cations (iron, calcium, aluminum, magnesium, selenium, zinc) in antacids, dairy products, mineral supplements: Eltrombopag chelates polyvalent cations, significantly reducing its absorption. Take eltrombopag tablets at least 2 hours before or 4 hours after any medications or products containing polyvalent cations.
- OATP1B1 substrates (e.g., atorvastatin, bosentan, ezetimibe, fluvastatin, glyburide, olmesartan, pitavastatin, pravastatin, rosuvastatin, repaglinide, rifampin, simvastatin acid, SN-38, valsartan): Eltrombopag may cause excessive exposure to substrates of OATP1B1. Use caution; monitor closely for signs and symptoms of excessive exposure and consider reducing the dose of these drugs if appropriate. In clinical trials a rosuvastatin dose reduction by 50% was recommended.
- BCRP substrates (e.g., imatinib, irinotecan, lapatinib, methotrexate, mitoxantrone, rosuvastatin, sulfasalazine, topotecan): Eltrombopag may cause excessive exposure to substrates of BCRP. Use caution; monitor closely for signs and symptoms of excessive exposure and consider reducing the dose of these drugs if appropriate.
- HIV protease inhibitors (lopinavir/ritonavir): No dose adjustment is recommended when coadministered with lopinavir/ritonavir; interactions with other HIV protease inhibitors have not been evaluated. No dose adjustment is recommended.
- Hepatitis C virus protease inhibitors (boceprevir, telaprevir): No dose adjustments are recommended when coadministered with boceprevir or telaprevir; interactions with other HCV protease inhibitors have not been evaluated. No dose adjustments are recommended.
- Peginterferon alfa-2a or -2b: No dose adjustments are recommended when coadministered with peginterferon alfa-2a or -2b. No dose adjustments are recommended.
- Clinical laboratory tests (bilirubin and creatinine): Eltrombopag is highly colored and can cause sample discoloration, interfering with bilirubin assays (positive and negative) and creatinine measurements (falsely elevated). If results are inconsistent with clinical observations or unexpected, evaluate liver or renal function further, communicate to the lab that the patient takes eltrombopag, and consider re-testing using other methods.
Read the label’s full interactions text
7 DRUG INTERACTIONS 7.1 Polyvalent Cations (Chelation) Eltrombopag chelates polyvalent cations (such as iron, calcium, aluminum, magnesium, selenium, and zinc) in foods, mineral supplements, and antacids. Take eltrombopag tablets at least 2 hours before or 4 hours after any medications or products containing polyvalent cations, such as antacids, dairy products, and mineral supplements to avoid significant reduction in absorption of eltrombopag tablets due to chelation [see Dosage and Administration (2.4), Clinical Pharmacology (12.3)] . 7.2 Transporters Use caution when concomitantly administering eltrombopag tablets and drugs that are substrates of OATP1B1 (e.g., atorvastatin, bosentan, ezetimibe, fluvastatin, glyburide, olmesartan, pitavastatin, pravastatin, rosuvastatin, repaglinide, rifampin, simvastatin acid, SN-38 [active metabolite of irinotecan], valsartan) or breast cancer resistance protein (BCRP) (e.g., imatinib, irinotecan, lapatinib, methotrexate, mitoxantrone, rosuvastatin, sulfasalazine, topotecan). Monitor patients closely for signs and symptoms of excessive exposure to the drugs that are substrates of OATP1B1 or BCRP and consider reduction of the dose of these drugs, if appropriate. In clinical trials with eltrombopag tablets, a dose reduction of rosuvastatin by 50% was recommended. 7.3 Protease Inhibitors HIV Protease Inhibitors: No dose adjustment is recommended when eltrombopag tablets are coadministered with lopinavir/ritonavir (LPV/RTV). Drug interactions with other HIV protease inhibitors have not been evaluated. Hepatitis C Virus Protease Inhibitors: No dose adjustments are recommended when eltrombopag tablets are coadministered with boceprevir or telaprevir. Drug interactions with other hepatitis C virus (HCV) protease inhibitors have not been evaluated. 7.4 Peginterferon Alfa-2a/b Therapy No dose adjustments are recommended when eltrombopag tablets are coadministered with peginterferon alfa-2a (PEGASYS ® ) or -2b (PEGINTRON ® ).
Excerpted — the section continues on the label. Read the full Drug Interactions section on DailyMed →
Not a complete list. The label covers the interactions the manufacturer studied or reported, and our own interaction database does not cover every medicine either. Bring your full medication list, including vitamins and herbal products, to your pharmacist.
Before taking Eltrombopag
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- Tell your prescriber about liver disease, hepatitis C, clotting risks, or MDS.
- Get an eye exam before starting.
- Pregnancy: can cause fetal harm; use effective contraception during treatment and for at least 7 days after.
- Breastfeeding is not recommended.
- Children: approved ages differ by product and condition.
- Older adults: no overall differences in safety or effectiveness were seen.
- Lower starting amounts may be needed with liver impairment or East-/Southeast-Asian ancestry for some conditions.
Eltrombopag overdose
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Too much can push platelet counts very high and cause blood clots. One reported large overdose led to a platelet count of 929 and also caused rash, slow heartbeat, liver test elevations, and fatigue. The label suggests taking a calcium-, aluminum-, or magnesium-containing product to limit absorption and closely monitoring platelets. Call Poison Help at 1-800-222-1222.
What Eltrombopag does in the body
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Eltrombopag raises platelet counts in a dose-dependent way with daily dosing. Counts peak about two weeks after starting and return to baseline about two weeks after the last dose. At doses up to the maximum recommended, it did not meaningfully affect the heart's QT interval.
How your body processes Eltrombopag
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Eltrombopag peaks 2 to 6 hours after a dose. A high-calcium meal sharply lowers absorption, which is why timing matters. It is heavily metabolized, mostly cleared in feces, and has a half-life of roughly 21 to 35 hours. Levels are higher in liver impairment and in people of East-/Southeast-Asian ancestry, and the oral suspension delivered about 22% more exposure than the tablet.
How to store Eltrombopag
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Store at room temperature between 20°C to 25°C (68°F to 77°F); excursions permitted between 15°C and 30°C (59°F and 86°F) . Dispense in original bottle.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Eltrombopag
55 supplements and herbal products have documented interactions with Eltrombopag in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 4
- Moderate · 42
- Minor · 9
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.
Eltrombopag: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Eltrombopag — the kind of thing our pharmacy team would talk through with you at the counter.
What is eltrombopag for?
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How should I take it?
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Why does it matter what I eat?
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What side effects should I expect?
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When should I call my doctor?
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Is it safe in pregnancy?
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Is Eltrombopag available over the counter?
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When was Eltrombopag first available?
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Who makes Eltrombopag?
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Answers drafted from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
More about Eltrombopag on HelloPharmacist
Eltrombopag forms and strengths (how it comes)
Eltrombopag 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.
Need a version that does not list lactose, a gluten source, a dye or gelatin? Inactive ingredients differ by manufacturer: see Eltrombopag inactive ingredients by manufacturer.
Tablet
How this form is used
- Eltrombopag tablets are used for ITP in patients 1 year and older, hepatitis C-related low platelets, and severe aplastic anemia including first-line use with immunosuppressive therapy.
- Alvaiz is used for ITP in patients 6 years and older, for chronic hepatitis C thrombocytopenia in adults, and for adults with severe aplastic anemia that did not respond enough to immunosuppressive therapy.
- Eltrombopag tablets are taken without a meal or with a meal low in calcium.
- Eltrombopag tablets are taken at least 2 hours before or 4 hours after antacids, calcium-rich foods, and mineral supplements.
- Alvaiz is not substitutable with other eltrombopag products on a milligram-for-milligram basis.
Oral suspension
How this form is used
- Eltrombopag for oral suspension is used for thrombocytopenia in persistent or chronic ITP in patients 1 year and older.
- Eltrombopag for oral suspension is used for thrombocytopenia in chronic hepatitis C so interferon-based therapy can start and continue.
- Eltrombopag for oral suspension is used for severe aplastic anemia that did not respond enough to immunosuppressive therapy.
- Eltrombopag for oral suspension is taken without a meal or with a meal low in calcium.
- Eltrombopag for oral suspension is taken at least 2 hours before or 4 hours after antacids, calcium-rich foods, and mineral supplements.
Eltrombopag on the U.S. market: products, makers and brands
How Eltrombopag 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.
14 companies list 68 Eltrombopag product records with the FDA, mostly as tablet, oral suspension; the earliest marketing or approval year on record is 2008. Brand names on the directory include Promacta, Alvaiz, Eltrombopag Olamine; the rest are generics.
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 (23) — 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 Eltrombopag is used (Medicaid data)
A general measure of how commonly Eltrombopag 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 Eltrombopag 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 Eltrombopag prescribed? Of the 1,601 medications we measure, Eltrombopag ranks #914 by Medicaid prescriptions — more than 43% of them.
Utilization by Eltrombopag 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.
eltrombopag 50 MG Oral Tablet Most dispensed
Summed across the 2 of 21 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 825427
eltrombopag 25 MG Oral Tablet
Summed across the 2 of 12 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 825421
eltrombopag 75 MG Oral Tablet
Summed across the 2 of 14 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 884617
eltrombopag 25 MG Powder for Oral Suspension
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1859498
eltrombopag 12.5 MG Oral Tablet
Summed across the 2 of 12 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 1245001
eltrombopag 18 MG Oral Tablet
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2675187
eltrombopag 36 MG Oral Tablet
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2675195
eltrombopag 54 MG Oral Tablet
Summed across the 1 of 1 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2675199
eltrombopag 12.5 MG Powder for Oral Suspension
Summed across the 2 of 6 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 2058980
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 Eltrombopag, 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 15 of 74 listed Eltrombopag NDCs with Medicaid activity.
Compare Eltrombopag products
A representative set of FDA-listed product records for Eltrombopag — 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 |
|---|---|---|---|---|
| 💊Oral suspension | ||||
| 12.5 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 25 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 💊Tablet | ||||
| 12.5 mg | Oral | Amerisyn, LLC | ANDA | View NDC → |
| 25 mg | Oral | Amerisyn, LLC | ANDA | View NDC → |
| 50 mg | Oral | Amerisyn, LLC | ANDA | View NDC → |
| 75 mg | Oral | Amerisyn, LLC | ANDA | View NDC → |
| 12.5 mg | Oral | Amneal Pharmaceuticals NY LLC × 2 listings | ANDA | View NDC → |
| 25 mg | Oral | Amneal Pharmaceuticals NY LLC × 2 listings | ANDA | View NDC → |
| 50 mg | Oral | Amneal Pharmaceuticals NY LLC × 2 listings | ANDA | View NDC → |
| 75 mg | Oral | Amneal Pharmaceuticals NY LLC × 2 listings | ANDA | View NDC → |
| 12.5 mg | Oral | AvKARE | ANDA | View NDC → |
| 25 mg | Oral | AvKARE | ANDA | View NDC → |
| 50 mg | Oral | AvKARE | ANDA | View NDC → |
| 75 mg | Oral | AvKARE | ANDA | View NDC → |
| 12.5 mg | Oral | Biocon Pharma Inc. | ANDA | View NDC → |
| 25 mg | Oral | Biocon Pharma Inc. | ANDA | View NDC → |
| 50 mg | Oral | Biocon Pharma Inc. | ANDA | View NDC → |
| 75 mg | Oral | Biocon Pharma Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 25 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 50 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 75 mg | Oral | Camber Pharmaceuticals, Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Dr. Reddy's Laboratories Inc., | ANDA | View NDC → |
| 25 mg | Oral | Dr. Reddy's Laboratories Inc., | ANDA | View NDC → |
| 50 mg | Oral | Dr. Reddy's Laboratories Inc., | ANDA | View NDC → |
| 75 mg | Oral | Dr. Reddy's Laboratories Inc., | ANDA | View NDC → |
| 12.5 mg | Oral | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 25 mg | Oral | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 50 mg | Oral | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 75 mg | Oral | Hikma Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Novadoz Pharmaceuticals LLC | ANDA | View NDC → |
| 25 mg | Oral | Novadoz Pharmaceuticals LLC | ANDA | View NDC → |
| 50 mg | Oral | Novadoz Pharmaceuticals LLC | ANDA | View NDC → |
| 75 mg | Oral | Novadoz Pharmaceuticals LLC | ANDA | View NDC → |
| 12.5 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 25 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 50 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 75 mg | Oral | Novartis Pharmaceuticals Corporation | NDA | View NDC → |
| 12.5 mg | Oral | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 25 mg | Oral | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 50 mg | Oral | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 75 mg | Oral | Somerset Therapeutics, LLC | ANDA | View NDC → |
| 9 mg | Oral | Teva Pharmaceuticals, Inc. | NDA | View NDC → |
| 12.5 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 18 mg | Oral | Teva Pharmaceuticals, Inc. | NDA | View NDC → |
| 25 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 36 mg | Oral | Teva Pharmaceuticals, Inc. | NDA | View NDC → |
| 50 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 54 mg | Oral | Teva Pharmaceuticals, Inc. | NDA | View NDC → |
| 75 mg | Oral | Teva Pharmaceuticals, Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | XLCare Pharmaceuticals Inc. | ANDA | View NDC → |
| 25 mg | Oral | XLCare Pharmaceuticals Inc. | ANDA | View NDC → |
| 50 mg | Oral | XLCare Pharmaceuticals Inc. | ANDA | View NDC → |
| 75 mg | Oral | XLCare Pharmaceuticals Inc. | ANDA | View NDC → |
| 12.5 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 25 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 50 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 75 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 12.5 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 25 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 50 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 75 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
Showing 68 of 68 products — FDA National Drug Code Directory. See every product, package size and price: browse all 68 Eltrombopag NDCs →
Eltrombopag side effects reported to the 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 Eltrombopag — 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 Eltrombopag 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.
Eltrombopag FDA approval history
How Eltrombopag went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Eltrombopag 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.
The FDA’s enforcement reports list no Eltrombopag recalls since July 2021.
✅No Eltrombopag recalls on record since July 2021Source: FDA enforcement (recall) reports, via openFDA; our copy was last updated Sep 24, 2026.
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 711942 2 dose forms · 10 strengths
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Dose form (SCDF) Oral Tablet RxCUI 825420In current FDA listings -
Dose form (SCDF) Powder for Oral Suspension RxCUI 1665882In current FDA listings
Look up RxCUI 711942 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.
Eltrombopag supply and shortage status
Whether Eltrombopag 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.
💵 What Eltrombopag costs pharmacies (NADAC benchmark)
The national average invoice price pharmacies pay for the drug itself, from CMS's NADAC survey (data as of Sep 30, 2026). This is a supply-cost benchmark — not a retail price and not what you'd pay at the counter.
| Form | Strength | Pharmacy acquisition benchmark | |
|---|---|---|---|
| Tablet · Oral | 50 mg | $25.85 per tablet | NDC details & price history |
Source: CMS National Average Drug Acquisition Cost (NADAC), a survey of retail pharmacy invoice prices. Benchmarks shown are the range across package sizes of a representative product for each form and strength — other manufacturers' products may differ.
Eltrombopag brand names
Eltrombopag is sold under 3 brand names in the FDA directory — Promacta, Alvaiz, Eltrombopag Olamine. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Eltrombopag: manufacturers and labelers
14 companies list Eltrombopag products with the FDA. By number of product records, the largest are Amneal Pharmaceuticals NY LLC, Teva Pharmaceuticals, Inc., Camber Pharmaceuticals, Inc.. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Eltrombopag drug class (RxNorm)
Eltrombopag belongs to the Thrombopoietin Receptor Agonist 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.
Sources for this Eltrombopag page
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 this page is built
HelloPharmacist combines public FDA and NLM records and does not author the underlying clinical facts. The plain-language sections are written with AI from the FDA-approved label text and reviewed by our pharmacy team before publication. Teva Pharmaceuticals, Inc. is the representative DailyMed label linked for verification and dates. This is general education, not medical advice: always talk to your doctor or pharmacist about your own medicines. How we build and review drug pages →