Bromocriptine
Bromocriptine is a dopamine-activating (ergot-derived) medicine used for hormone-related conditions such as high prolactin levels and acromegaly, for Parkinson's disease, and, in the Cycloset brand, for type 2 diabetes.
🧬 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 10 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 →
Bromocriptine is an older, ergot-derived medicine that mimics dopamine to lower high prolactin and excess growth hormone (acromegaly) and to stimulate dopamine-starved movement areas in Parkinson's disease, on the market since about 1978 and available generically; a separate brand, Cycloset, is used for type 2 diabetes. Nausea is what most people notice, plus dizziness and headache, early on, which is why doses start low and are taken with food. The serious risk is scarring (fibrosis) of heart valves and lungs, so expect heart ultrasounds (echocardiograms) before and during treatment, and report chest pain, breathlessness, a lasting cough or swelling. Sudden sleep episodes or a severe headache also need prompt attention.
Clinical pearls
- Take each dose with food, because vomiting is far more common on an empty stomach.
- Cycloset is taken once each morning within two hours of waking; a missed dose is skipped, never doubled.
- Avoid ergot migraine drugs with it, and know that metoclopramide or antipsychotics can cancel out its effect.
- It should never be used to dry up breast milk after delivery, a use linked to stroke, seizures and heart attack.
Patient information guide A plain-language walkthrough of Bromocriptine, written from its FDA label.
What Bromocriptine is used for
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Bromocriptine mesylate is used for several hormone and nerve-related conditions, and one brand is used for diabetes.
- High-prolactin dysfunction: missed periods with or without milk discharge, infertility or low sex hormone levels (hypogonadism).
- Prolactin-secreting pituitary tumors (adenomas), including use before surgery to shrink the tumor.
- Acromegaly, alone or alongside pituitary radiation or surgery.
- Idiopathic or postencephalitic Parkinson's disease, often added to levodopa.
- Cycloset tablets only: type 2 diabetes in adults, with diet and exercise.
How Bromocriptine works
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Bromocriptine activates dopamine receptors. In the pituitary gland, this lowers prolactin. In acromegaly, it also lowers high growth hormone.
In Parkinson's disease, it directly stimulates dopamine receptors in the brain's movement-control area. This differs from levodopa, which must first be converted to dopamine.
Bromocriptine dosage
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Bromocriptine mesylate capsules and tablets are taken by mouth with food. Doses usually start low and are increased gradually. Follow your prescriber and the product label.
- High prolactin and adenomas: generally once daily.
- Acromegaly: usually started at bedtime with food.
- Parkinson's disease: generally twice daily.
- Cycloset: once daily within two hours of waking, with food. If you miss a dose, take your usual dose the next morning and do not double up.
Dosing details from the FDA-approved label
From the Bromocriptine 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.
- Hyperprolactinemia-associated dysfunction in adults
- 1.25 mg (one-half of a tablet) to 2.5 mg once daily
- Increase up to 2.5 mg once daily every two to seven days as tolerated until an optimal therapeutic response is achieved
- Maximum: 2.5 mg to 15 mg once daily (recommended dosage range)
- Take with food
- Prolactin-secreting adenomas in adult and pediatric patients 11 years of age and older
- 1.25 mg (one-half of a tablet) to 2.5 mg once daily
- Increase as tolerated until an optimal therapeutic response is achieved
- Maximum: 2.5 mg to 10 mg once daily (recommended dosage range)
- Take with food
- Acromegaly in adults
- 1.25 mg (one-half of a tablet) to 2.5 mg once at bedtime for 3 days
- Then increase by 1.25 mg to 2.5 mg once daily every 3 days to 7 days as tolerated
- Usual optimal range 20 mg to 30 mg once at bedtime in most patients
- Maximum: 100 mg/daily
- Take with food
- Idiopathic Parkinson's disease or postencephalitic parkinsonism in adults
- 1.25 mg (one-half of a tablet) twice daily
- Increase by 1.25 mg twice daily every 14 days to 28 days based on therapeutic response and tolerability
- Maximum: 100 mg/day
- Take with food
- Hyperprolactinemia-associated dysfunction in adults with concomitant moderate CYP3A4 inhibitors
- Starting dosage 1.25 mg once daily (one-half of a tablet)
- Maximum: 3.75 mg once daily
- Dosage modification for moderate CYP3A4 inhibitors
- Prolactin-secreting adenomas in adult and pediatric patients 11 years of age and older with concomitant moderate CYP3A4 inhibitors
- Starting dosage 1.25 mg once daily
- Maximum: 2.5 mg once daily
- Dosage modification for moderate CYP3A4 inhibitors
- Acromegaly in adults with concomitant moderate CYP3A4 inhibitors
- Starting dosage 1.25 mg once daily
- Maximum: 25 mg once daily
- Dosage modification for moderate CYP3A4 inhibitors
- Idiopathic or postencephalitic parkinsonism in adults with concomitant moderate CYP3A4 inhibitors
- Starting dosage 1.25 mg once daily
- Maximum: 12.5 mg twice daily
- Dosage modification for moderate CYP3A4 inhibitors
Read the label’s full dosing text
2 DOSAGE AND ADMINISTRATION Before initiating bromocriptine mesylate capsules, evaluate for valvular heart disease, including with an echocardiogram. If valvular disease is detected, do not administer bromocriptine mesylate ( 2.1 ). Take bromocriptine mesylate capsules orally with food ( 2.2 ) Recommended dosage for hyperprolactinemia-associated dysfunction is 1.25 mg (one-half of a tablet) to 2.5 mg once daily. Increase the dosage up to 2.5 mg once daily every two to seven days within a recommended dosage of 2.5 mg to 15 mg once daily ( 2.3 ) Recommended dosage for prolactin-secreting adenomas is 1.25 mg to 2.5 mg once daily. Increase the dosage within a recommended dosage of 2.5 mg to 10 mg once daily ( 2.4 ) Recommended dosage for acromegaly is 1.25 mg to 2.5 mg once at bedtime for 3 days. Increase the dosage 1.25 mg to 2.5 mg once daily every 3 days to 7 days up to the maximum recommended dosage is 100 mg/daily ( 2.5 ). Recommended starting dosage for idiopathic or postencephalitic Parkinson's disease is 1.25 mg twice daily. Increase the dosage by 1.25 mg twice daily every 14 days to 28 days up to the maximum recommended daily dosage of 100 mg/day ( 2.6 ) For dosage modifications for concomitant use of bromocriptine mesylate with moderate CYP3A4 inhibitors, see Full Prescribing Information ( 2.7 , 7 ) 2.1 Recommended Evaluation Before Initiating bromocriptine mesylate Before initiating bromocriptine mesylate evaluate for valvular heart disease, including with an echocardiogram. If valvular disease is detected, do not administer bromocriptine mesylate [see Contraindications ( 4 ) and Warnings and Precautions ( 5.1 )] . 2.2 Important Administration Instructions Take bromocriptine mesylate orally with food because a high percentage of patients vomited after they received bromocriptine mesylate under fasting conditions. 2.3 Recommended Dosage for Hyperprolactinemia-Associated Dysfunction The recommended starting dosage of bromocriptine mesylate in adults with hyperprolactinemia-associated dysfunction is 1.25 mg (one-half of a tablet) to 2.5 mg once daily. Increase the bromocriptine mesylate dosage up to 2.5 mg once daily every two to seven days as tolerated until an optimal therapeutic response is achieved within a recommended dosage of 2.5 mg to 15 mg once daily.
Excerpted — the section continues on the label. Read the full Dosage and Administration section on DailyMed →
Bromocriptine side effects
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Side effects are common but are usually mild to moderate.
Common side effects
- Nausea
- Headache
- Dizziness or lightheadedness
- Tiredness
- Vomiting
- Constipation
- Nasal congestion
- Drowsiness
- Abdominal cramps
- Constipation or diarrhea
When to get medical help
- Sudden sleep episodes or severe daytime sleepiness: avoid driving and tell your doctor right away.
- Severe or worsening headache, especially with vision changes, high blood pressure or seizures: get medical help promptly.
- Chest pain, new shortness of breath, swelling in the legs or signs of heart failure: these can signal heart valve or fibrosis problems.
- Persistent cough, back or flank pain, or leg swelling: these can signal fibrosis in the lungs or abdomen.
- Dizziness or fainting when you stand up: low blood pressure can happen, especially early in treatment.
- New gambling, spending, eating or sexual urges that are hard to control: tell your doctor.
- Hallucinations, confusion or worsening psychosis.
- Worsening vision, such as loss of visual field, if you have a pituitary tumor.
Call your doctor about sudden sleep episodes, fainting, severe headache, vision changes, chest pain, breathing problems, hallucinations or compulsive urges.
Bromocriptine warnings and precautions
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- Heart valve and heart-lining fibrosis: your doctor checks your heart before and during treatment.
- Fibrosis in the lungs, chest lining or abdomen has been reported, especially with long-term, high-dose use.
- Low blood pressure, especially early in treatment or when standing.
- Sudden sleep onset, which can cause accidents while driving.
- Impulse-control problems such as gambling, spending, binge eating or sexual urges.
- Not recommended for stopping milk production after birth. This has been linked to high blood pressure, seizures, stroke, heart attack and death.
- Vision changes may occur with pituitary tumors, so visual fields should be monitored.
- It can worsen severe psychotic disorders.
Bromocriptine interactions
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Bromocriptine can clash with several drug types.
- Other ergot drugs: more ergot side effects and less migraine benefit.
- Antipsychotics and metoclopramide: they block dopamine and can cancel out bromocriptine.
- CYP3A4 inhibitors such as azole antifungals, HIV protease inhibitors and erythromycin: they can raise bromocriptine levels.
- Sympathomimetics and sumatriptan-type drugs: caution advised with Cycloset.
- Drugs that change blood pressure: use with caution.
- Highly protein-bound drugs such as salicylates: Cycloset may change their effects.
Interactions listed in the FDA-approved label
From the Bromocriptine prescribing information (“Drug Interactions”): what the manufacturer studied or reported to the FDA.
- Highly protein-bound drugs (e.g., salicylates, sulfonamides, chloramphenicol, probenecid): May increase the unbound fraction of these drugs, which may alter their effectiveness and risk for side effects.
- Dopamine receptor antagonists (neuroleptics such as phenothiazines, butyrophenones, thioxanthenes; metoclopramide): May diminish the effectiveness of bromocriptine, and bromocriptine may diminish the effectiveness of these therapies. Concurrent use has not been studied in clinical trials and is not recommended.
- Ergot-related drugs: May increase ergot-related side effects such as nausea, vomiting, and fatigue, and may reduce the effectiveness of ergot therapies used to treat migraine. Concurrent use of ergot agents within 6 hours of dosing is not recommended.
- Moderate CYP3A4 inhibitors (e.g., erythromycin): May increase circulating levels of bromocriptine, which is extensively metabolized by CYP3A4. Use caution; dose should not exceed 1.6 mg once daily during concomitant use.
- Strong CYP3A4 inhibitors (e.g., azole antimycotics, HIV protease inhibitors): May increase circulating levels of bromocriptine. Avoid concomitant use; ensure adequate washout of the strong inhibitor before initiating treatment.
- CYP3A4 inducers: May reduce circulating levels of bromocriptine. Use caution when co-administering.
- Sympathomimetic drugs (e.g., phenylpropanolamine, isometheptene): Postmarketing reports of hypertension and tachycardia when co-administered in postpartum women; limited safety data for use longer than 10 days. Concomitant use for more than 10 days is not recommended.
- Selective 5-HT1B agonists (e.g., sumatriptan): There are limited clinical trial data supporting the safety of concurrent use. Concomitant use should be avoided.
Read the label’s full interactions text
7 DRUG INTERACTIONS The active ingredient in CYCLOSET (bromocriptine mesylate) is highly bound to serum proteins. Therefore, CYCLOSET may increase the unbound fraction of other concomitantly used highly protein-bound therapies (e.g., salicylates, sulfonamides, chloramphenicol and probenecid), which may alter their effectiveness and risk for side effects. CYCLOSET is a dopamine receptor agonist. Concomitant use of dopamine receptor antagonists, such as neuroleptics (e.g., phenothiazines, butyrophenones, thioxanthenes), or metoclopramide may diminish the effectiveness of CYCLOSET, and CYCLOSET may diminish the effectiveness of these other therapies. The concurrent use of CYCLOSET with these agents has not been studied in clinical trials and is not recommended [see Warnings and Precautions (5.5) ]. CYCLOSET in combination with ergot-related drugs may cause an increase in the occurrence of ergot-related side effects, such as nausea, vomiting, and fatigue, and may also reduce the effectiveness of these ergot therapies when used to treat migraine. The concurrent use of these ergot agents within 6 hours of CYCLOSET dosing is not recommended. CYCLOSET is extensively metabolized by the liver via CYP3A4. Therefore, potent inhibitors or inducers of CYP3A4 may increase or reduce the circulating levels of CYCLOSET, respectively. Use caution when co-administering drugs that are inhibitors or inducers of CYP3A4. CYCLOSET dose should not exceed 1.6 mg once daily during concomitant use of a moderate CYP3A4 inhibitor (e.g., erythromycin). Concomitant use of strong CYP3A4 inhibitors (e.g., azole antimycotics, HIV protease inhibitors) with CYCLOSET should be avoided. Ensure adequate washout of the strong CYP3A4 inhibitor drug before initiating CYCLOSET treatment [see Clinical Pharmacology (12.3) ] .
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 Bromocriptine
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- Not for use with heart valve disease, pericardial fibrosis, or a history of lung or abdominal fibrosis.
- Not for use with uncontrolled high blood pressure or ergot sensitivity.
- Pregnancy: for high prolactin, it is generally stopped once pregnancy is diagnosed. Use contraception as advised and have regular pregnancy tests while periods are absent.
- Avoid while breastfeeding in postpartum females.
- Children 11 and older can use it for prolactin-secreting adenomas. It has not been established for other uses in children.
- Liver problems: levels may rise, so caution is needed.
- Contains lactose, so avoid with certain hereditary sugar-intolerance conditions.
Bromocriptine overdose
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Overdose can cause nausea, vomiting, dizziness, severe low blood pressure, confusion, drowsiness, hallucinations and repetitive yawning. Treatment includes removing the drug from the stomach, activated charcoal, fluids and monitoring. Seek emergency help or call poison control right away.
What Bromocriptine does in the body
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In the Cycloset diabetes trials, once-daily Cycloset improved after-meal blood sugar without raising insulin levels. It also improved how the body uses insulin to clear glucose, with lower blood sugar and HbA1c.
How your body processes Bromocriptine
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Bromocriptine peaks in the blood in about 2.5 hours and has a half-life of about 5 hours. Food did not significantly change how much is absorbed, but taking it with food reduces vomiting. It is heavily processed in the liver by the CYP3A4 enzyme. Most of it leaves through the stool and a small amount through urine.
How to store Bromocriptine
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Store and dispense: At 20-25°C (68-77°F) in a tight, light-resistant container.
Written from the FDA-approved label with AI and reviewed by our pharmacy team. How we use AI →
Supplements & herbs that interact with Bromocriptine
143 supplements and herbal products have documented interactions with Bromocriptine in the licensed clinical database we use. Most are manageable — but your pharmacist should know about everything you take, including vitamins and herbals.
- Major · 3
- Moderate · 99
- Minor · 41
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.
Bromocriptine: pharmacist answers to common questions
Quick, plain-English answers to the questions patients ask most about Bromocriptine — the kind of thing our pharmacy team would talk through with you at the counter.
What is bromocriptine for?
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Should I take it with food?
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What side effects should I expect?
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When should I call my doctor?
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Can I take it if I'm pregnant or breastfeeding?
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What medicines should I be careful with?
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Is Bromocriptine available over the counter?
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When was Bromocriptine first available?
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Who makes Bromocriptine?
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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 Bromocriptine on HelloPharmacist
Bromocriptine forms and strengths (how it comes)
Bromocriptine 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.
Tablet
How this form is used
- Bromocriptine mesylate tablets are used for high-prolactin dysfunction, prolactin-secreting adenomas, acromegaly and Parkinson's disease.
- Cycloset tablets are used with diet and exercise to improve blood sugar control in adults with type 2 diabetes.
- Parlodel tablets (SnapTabs) are used for the same conditions as bromocriptine mesylate tablets.
- Bromocriptine mesylate tablets are taken with food.
- Cycloset is taken once daily within two hours after waking, with food.
- If a morning dose of Cycloset is missed, take the usual dose the next morning and do not double it.
Capsule
How this form is used
- Bromocriptine Mesylate capsules are used for high-prolactin dysfunction, prolactin-secreting adenomas, acromegaly and Parkinson's disease.
- Parlodel capsules are used for the same conditions.
- Bromocriptine Mesylate capsules are taken by mouth with food.
- Bromocriptine Mesylate capsules require a heart valve evaluation before starting.
Bromocriptine on the U.S. market: products, makers and brands
How Bromocriptine 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.
9 companies list 10 Bromocriptine product records with the FDA, mostly as tablet, capsule; the earliest marketing or approval year on record is 1978. Brand names on the directory include Cycloset, Parlodel; 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 (5) — 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 Bromocriptine is used (Medicaid data)
A general measure of how commonly Bromocriptine 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 Bromocriptine 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 Bromocriptine prescribed? Of the 1,601 medications we measure, Bromocriptine ranks #834 by Medicaid prescriptions — more than 48% of them.
Utilization by Bromocriptine 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.
bromocriptine 2.5 MG Oral Tablet Most dispensed
Summed across the 5 of 20 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 197411
bromocriptine 5 MG Oral Capsule
Summed across the 3 of 14 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 197412
bromocriptine 0.8 MG Oral Tablet
Summed across the 1 of 4 listed NDC products with Medicaid activity — every brand and generic of this exact strength & form. RxNorm 859077
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 Bromocriptine, 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 9 of 38 listed Bromocriptine NDCs with Medicaid activity.
Compare Bromocriptine products
A representative set of FDA-listed product records for Bromocriptine — 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 |
|---|---|---|---|---|
| 💊Capsule | ||||
| 5 mg | Oral | ANI Pharmaceuticals, Inc. | NDA | View NDC → |
| 5 mg | Oral | Mylan Pharmaceuticals Inc. | ANDA | View NDC → |
| 5 mg | Oral | Zydus Lifesciences Limited | ANDA | View NDC → |
| 5 mg | Oral | Zydus Pharmaceuticals USA Inc. | ANDA | View NDC → |
| 💊Tablet | ||||
| 2.5 mg | Oral | American Health Packaging | NDA | View NDC → |
| 2.5 mg | Oral | ANI Pharmaceuticals, Inc. | NDA | View NDC → |
| 0.8 mg | Oral | Avvisto Therapeutics LLC | NDA | View NDC → |
| 2.5 mg | Oral | Padagis US LLC | ANDA | View NDC → |
| 2.5 mg | Oral | Remedyrepack Inc. | ANDA | View NDC → |
| 2.5 mg | Oral | Sandoz Inc | ANDA | View NDC → |
Showing 10 of 10 products — FDA National Drug Code Directory. See every product, package size and price: browse all 10 Bromocriptine NDCs →
Bromocriptine 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 Bromocriptine — 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 Bromocriptine 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.
Bromocriptine FDA approval history
How Bromocriptine went from FDA review to the pharmacy shelf — the key milestones in its regulatory journey.
Source: Drugs@FDA.
Bromocriptine 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 one Bromocriptine recall since July 2021. It is still ongoing. A recall names specific lots from one company, so check the lot number on your own bottle rather than assuming every product is affected; your pharmacist can check whether your supply came from an affected lot.
- Bromocriptine Mesylate Capsules, USP, 5 mg, 30 Capsules per bottle, Rx Only. Manufactured by: Zydus Lifesciences Ltd., Ahmedabad, India. Distributed by: Zydus Pharmaceuticals, Pennington, NJ 08534. N… Lots: Lot #: M313934, M313935, M315615, Exp. Date Nov 2025; M316809 , Exp. Date Dec-25; M405765, M405763, M405764, Exp. Date Apr-26; M414999, M414241, M414307, M414305, Exp. Date Oct-26 FDA record D-0159-2026 →
Source: 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 1760 2 dose forms · 5 strengths
-
Dose form (SCDF) Oral Capsule RxCUI 371127In current FDA listings -
Dose form (SCDF) Oral Tablet RxCUI 371128In current FDA listings
Look up RxCUI 1760 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.
Bromocriptine supply and shortage status
Whether Bromocriptine 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 Bromocriptine 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 | 2.5 mg | $1.61 per tablet | NDC details & price history |
| Tablet · Oral | 0.8 mg | $5.26 per tablet | NDC details & price history |
| Capsule · Oral | 5 mg | $4.12 per capsule | 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.
Bromocriptine brand names
Bromocriptine is sold under 2 brand names in the FDA directory — Cycloset, Parlodel. A brand and its generic contain the same active ingredient; the brand name belongs to one company's product.
Who makes Bromocriptine: manufacturers and labelers
9 companies list Bromocriptine products with the FDA. By number of product records, the largest are ANI Pharmaceuticals, Inc., American Health Packaging, Avvisto Therapeutics LLC. Labelers include manufacturers and repackagers; the product in your bottle depends on which one your pharmacy stocks.
Bromocriptine drug class (RxNorm)
Bromocriptine belongs to the Ergot Derivative 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 Bromocriptine 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. Avvisto Therapeutics LLC 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 →