Benefits
Selected reproductive/endocrine indications; the label explicitly rejects claims of effectiveness for obesity.
Named U.S. presentation only; selected label sections.
Peptide library
Your guide to this compound.


The named U.S. product label is the appropriate source for its approved use, contraindications and handling. The selected PREGNYL label does not supply a numerical human elimination half-life. Hormonal effects and data for recombinant chorionic gonadotropin cannot substitute for a matched estimate for this urinary-derived product. A label extraction is not an independent appraisal of every supporting trial or approval of other products with the same ingredient.
Named U.S. product label sections assessed.
Product-specific editorial extraction. Complete clinical review and clinician sign-off remain pending; other jurisdictions are not inferred.
Editorial assessment · 2026-09-07
The population specified by this product label; other indications and jurisdictions remain outside this check.
Selected reproductive/endocrine indications; the label explicitly rejects claims of effectiveness for obesity.
U.S. label record for BLA017692. This does not confer authorization on other products using the ingredient name.
Named-product label sections were expanded for pharmacokinetics, contraindications and selected handling or interaction details on September 7, 2026. This is not a complete trial-program appraisal or clinician sign-off. Other formulations, patient-specific decisions and other jurisdictions require separate assessment.
PREGNYL chorionic gonadotropin, 10,000 USP-unit multidose vial
Consult the product label for pharmacology. A mechanism does not extend its approved indications.
Approval applies to a particular product and indication. It does not extend to every use, route, compounded preparation or research vial sold under the same compound name. Check the current prescribing information.
Named U.S. presentation only; selected label sections.
Approval applies to a particular product and indication. It does not extend to every use, route, compounded preparation or research vial sold under the same compound name. Check the current prescribing information.
Selected reproductive/endocrine indications; the label explicitly rejects claims of effectiveness for obesity.
Named U.S. presentation only; selected label sections.
Fertility treatment requires ovarian-response monitoring and assessment of hypersensitivity and hyperstimulation risks.
Named U.S. presentation only; selected label sections.
PREGNYL: unopened 15–30°C; after reconstitution refrigerate 2–8°C and discard after 60 days. Do not shake or freeze.
Named U.S. presentation only; selected label sections.
The selected PREGNYL label does not supply a numerical human elimination half-life. Hormonal effects and data for recombinant chorionic gonadotropin cannot substitute for a matched estimate for this urinary-derived product.
Named U.S. product only; label revision 20240218. Educational extraction, not complete clinical review.
PREGNYL: gonadotropin/excipient hypersensitivity; primary ovarian failure; uncontrolled thyroid/adrenal/pituitary disorders; specified hormone-dependent or hypothalamic/pituitary tumors; reproductive malformations or fibroids incompatible with pregnancy; unexplained vaginal bleeding.
Named U.S. product only; label revision 20240218. Educational extraction, not complete clinical review.
Low-dose human chorionic gonadotropin maintains intratesticular testosterone in normal men with testosterone-induced gonadotropin suppression. 2005.
PMID: 15713727
PREGNYL chorionic gonadotropin, 10,000 USP-unit multidose vial. U.S. structured product label, effective 20240218. Selected sections only.
Catalog review date: Sep 7, 2026. This date alone does not establish independent clinical review.