Key facts
- Active ingredient
- Cetrorelix Acetate
- Form
- Kit
- Strength
- Cetrorelix Acetate EQ 0.25MG BASE/VIAL
- Type
- Prescription (Rx)
- Brand or generic
- Generic
- May treat
- ovarian hyperstimulation syndrome
- Manufacturer
- Humanwell
- FDA application
- ANDA218740
May treat (source: NIH RxClass)
Dosage forms
Kit
The forms currently marketed in the U.S., per the FDA National Drug Code Directory.
Ways to save
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Use copay cards
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Frequently asked questions
- What does Cetrorelix Acetate treat?
- Cetrorelix Acetate (Cetrorelix Acetate) may be used to treat ovarian hyperstimulation syndrome, based on NIH RxClass drug-classification data (conditions a drug may treat — not a verbatim copy of the FDA-approved label). This is general reference, not medical advice.
- Is there a coupon or discount for Cetrorelix Acetate?
- pharmaranks is an independent ratings site, not a pharmacy — we don't issue coupons or sell Cetrorelix Acetate. To pay less, Cetrorelix Acetate is already a generic — usually the lowest-cost version — so the main levers are comparing cash prices between pharmacies and using a pharmacy discount-card service. Prices vary by pharmacy, insurance, and location, so always confirm at the counter. This is general reference, not medical or financial advice.
- Who makes Cetrorelix Acetate?
- Cetrorelix Acetate is marketed by Humanwell. You can see Humanwell's full profile, rating, and other products on pharmaranks.
- Is Cetrorelix Acetate a brand-name or generic drug?
- Cetrorelix Acetate is a generic medication; its active ingredient is Cetrorelix Acetate. Generics contain the same active ingredient as the brand-name original and are usually lower cost.
- Is Cetrorelix Acetate available over the counter?
- No. Cetrorelix Acetate is a prescription (Rx) medication in the US — you need a prescription from a licensed clinician (in person or via telehealth); it isn't sold over the counter. For some conditions there are OTC alternatives — ask your pharmacist.
- What forms does Cetrorelix Acetate come in?
- Cetrorelix Acetate is currently marketed as kit, per the FDA's National Drug Code Directory.
- Is Cetrorelix Acetate FDA-registered?
- Cetrorelix Acetate is on record with the U.S. FDA under application number ANDA218740. You can verify this on its official FDA label.
Information is sourced from public FDA regulatory data. Provided for general reference only — not medical advice. Always consult a licensed professional and the current prescribing information.
What people report to the FDA about Cetrorelix Acetate
The FDA Adverse Event Reporting System (FAERS) collects reports from patients and clinicians. It holds 102 reports naming Cetrorelix Acetate, and the FDA flagged 81% of those reports as serious. The effects reported most often — leaving out reports about overdose, misuse or the condition being treated, which dominate the raw list for common medicines:
- ovarian hyperstimulation syndrome21 reports
- generalised tonic-clonic seizure19 reports
- drug level decreased18 reports
- blood oestrogen increased10 reports
- abortion spontaneous8 reports
- ascites6 reports
- abdominal pain5 reports
- pleural effusion5 reports
Read these as a signal, not a rate. A report does not mean Cetrorelix Acetate caused the effect — anyone can file one, and many describe people taking several medicines for several conditions. Crucially there is no denominator: FAERS does not record how many people took the drug, so these counts cannot be turned into “X% of patients” — a bigger number often just means a more widely used or more talked-about drug. Duplicates exist, and publicity drives reporting. For what is actually established, read the FDA label.
Source: openFDA drug/event (FAERS), retrieved September 25, 2026.
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