FDA LABEL RECORD
GANIRELIX ACETATE
GANIRELIX ACETATE. FDA prescribing information for this product, as published on the retrieval date below.
AS THE LABEL RECORDS IT
Product details
| Brand name | GANIRELIX ACETATE |
|---|---|
| Generic name | GANIRELIX ACETATE |
| Labeller | Gland Pharma Limited |
| Route | SUBCUTANEOUS |
| Label version | 3 |
| Effective | 2023-11-29 |
| Retrieved by this site | 2026-10-03 |
| Full label | https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=cad7c09c-234b-4e73-b460-a1b1f7adc28d |
INDICATIONS AND USAGE
Quoted from the FDA label
INDICATIONS AND USAGE Ganirelix Acetate Injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian hyperstimulation.
What this page is
A reproduction of a public FDA label record. Everything quoted above is the labeller's wording as published by the FDA, not this site's. Nothing here is regulatory, legal or medical advice, and a label being reproduced says nothing about whether a product is available in any particular country. Labels are revised often; the retrieval date above says when this copy was taken, and the full current label is at the link.
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