Peptide Medix product catalog

Peptide Medix

HMG (Menotropins) 75 IU — Prescription Reference

Urinary-derived gonadotropin preparation with FSH and LH activity — Rx only

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Overview

This is a prescription-only biologic listed for institutional reference. Human menopausal gonadotropin, or menotropins, is supplied only against a valid prescription or documented institutional authorisation, and this entry exists so that catalogue users can see specification and handling information. It is not offered for open sale, and no sourcing, dosing or administration guidance is provided here.

Menotropins is a gonadotropin preparation purified from the urine of postmenopausal women, catalogued under CAS 61489-71-2 and standardised by bioassay rather than by mass. A conventional vial supplies 75 IU of follicle-stimulating hormone activity together with 75 IU of luteinising hormone activity. Both are glycoprotein hormones sharing a common alpha subunit with a hormone-specific beta subunit, and in highly purified preparations a portion of the LH activity is contributed by chorionic gonadotropin present in the source material — which is why potency is expressed in international units against a reference standard.

Specifications

Brand Peptide Medix
Category Prescription Hormones
Regulatory status Prescription-only medicine; supplied exclusively against valid prescription or institutional authorisation
Product type Human menopausal gonadotropin (menotropins), a urinary-derived glycoprotein hormone preparation
Available sizes 75 IU vial; 75 IU × 5 pack
Potency basis International units assigned by bioassay against an international reference standard, not by mass
Activity per vial 75 IU follicle-stimulating hormone activity with 75 IU luteinising hormone activity
CAS number 61489-71-2
Source Purified from urine of postmenopausal women
Molecular nature Heterodimeric glycoprotein hormones — a common alpha subunit paired with a hormone-specific beta subunit, extensively glycosylated
Receptor targets FSH receptor and the luteinising hormone/choriogonadotropin receptor (LHCGR)
Form Lyophilized powder in a sealed vial, reconstituted with the supplied or specified diluent
Approved indication areas Assisted reproductive technology and, per individual product licence, ovulation induction — as stated in approved labelling
Storage (lyophilized) Per approved labelling — commonly refrigerated or at controlled room temperature, protected from light
Storage (reconstituted) Refrigerated and used within the period stated in the approved labelling
Supply condition Dispensed only against valid authorisation; no dosing or administration guidance supplied by MyPeptide
SKU HMG-75-IU-VIAL

Highlights

  • Prescription-only biologic — supplied solely against valid authorisation, listed here for reference
  • Urinary-derived gonadotropin standardised by bioassay in international units
  • 75 IU vial delivering FSH activity together with LH activity
  • Glycoprotein hormones: shared alpha subunit with hormone-specific beta subunits
  • Approved indications centre on assisted reproductive technology and ovulation induction
  • Pharmacologically distinct from recombinant FSH-only preparations
  • Lyophilized powder requiring reconstitution; refrigerated storage after mixing
  • No dosing, protocol or sourcing guidance is provided with this listing

What's Included

  • The vial option and size selected above
  • Final item and quantity confirmed in cart
  • Laboratory-research-use labeling

Research Overview

What menotropins actually is

Unlike a synthetic peptide, menotropins is a purified biological preparation. Postmenopausal urine contains elevated gonadotropins because the negative feedback from ovarian steroids has been removed, and the manufacturing process concentrates and purifies that material to a defined activity. The result is not a single molecular entity: it contains glycoprotein hormone isoforms differing in glycosylation, and this heterogeneity is exactly why potency must be assigned by bioassay in international units rather than measured as milligrams of active substance.

Two activities, two receptors

FSH acts at the FSH receptor on granulosa cells, driving follicular growth and aromatase expression. LH activity acts at LHCGR on theca and, later, granulosa cells, supplying the androgen precursors that aromatase converts to oestradiol and triggering the events of ovulation and luteinisation. The two-cell two-gonadotropin model of ovarian steroidogenesis is the standard framework for understanding why a preparation containing both differs from one containing FSH alone. In highly purified menotropin products, part of the measured LH activity is contributed by chorionic gonadotropin from the source material, since hCG acts at the same receptor with a longer circulating half-life.

  • Approved in the United States and other jurisdictions for use in assisted reproductive technology, with ovulation induction included in some product licences
  • Ovarian hyperstimulation syndrome and multiple gestation are recognised risks addressed in approved labelling
  • Comparative literature examines urinary menotropins against recombinant FSH across oocyte yield, oestradiol profile and cycle outcome measures

Why the recombinant comparison recurs

HMG (Menotropins) 75 IU — Prescription Reference FAQ

Can I buy HMG from this page?
No. This is a prescription-only biologic and this entry is a reference listing for institutional catalogue use. It can be supplied only against a valid prescription or documented institutional authorisation, and we provide no sourcing route, dosing information or administration guidance for it.
Why is HMG measured in IU rather than milligrams?
Because it is a purified biological preparation containing heterogeneously glycosylated glycoprotein isoforms, equal masses do not carry equal biological activity. International units assigned by bioassay against an international reference standard express activity directly, and the assayed value for the specific lot is what governs.
What are its approved uses?
As a matter of public regulatory record, menotropin products are approved for use in assisted reproductive technology — development of multiple follicles in appropriately selected patients — and, depending on the individual product licence, for ovulation induction. Approved labelling for the specific product is the authoritative source.
How does it differ from recombinant FSH?
Recombinant FSH is produced in cell culture and contains FSH activity only. Menotropins is purified from urine and delivers both FSH and LH activity, with part of the LH activity in highly purified products contributed by chorionic gonadotropin from the source. That pharmacological difference is the subject of most published comparisons.
How does it relate to HCG and gonadorelin?
All three act on the reproductive axis at different points. Gonadorelin is GnRH, acting on the pituitary upstream; HCG is an LHCGR agonist with a long half-life; menotropins delivers both FSH and LH activity directly to the gonad. They are pharmacologically distinct and not interchangeable.
What documentation accompanies a supplied vial?
Where supply is authorised, vials arrive with manufacturer labelling stating assayed potency in international units, lot number and expiry, together with the approved product information. Documentation, storage and dispensing records are handled under the receiving institution's own quality controls.

This catalog listing is for laboratory research use only. It is not represented as a drug, food, supplement, cosmetic or diagnostic product, and it is not offered for human or veterinary use.

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