A parathyroid-hormone fragment studied in research on bone-metabolism pathways.
Evidence brief
Teriparatide is a recombinant fragment of human parathyroid hormone (rhPTH 1-34) approved as an anabolic (bone-forming) osteoporosis medicine, and it has been studied in many randomized controlled trials and pooled in meta-analyses.
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▸ Regulatory statusUSapprovedEUapprovedUKapproved
An approved prescription medicine for osteoporosis: FDA-approved as Forteo (NDA 021318) for postmenopausal women and men at high risk of fracture and for glucocorticoid-induced osteoporosis, centrally authorised in the EU as Forsteo, and authorised in the UK. Approved for osteoporosis only — not for any performance, recovery or anti-ageing use. Research use only — not medical advice.
Teriparatide is a recombinant fragment of human parathyroid hormone (rhPTH 1-34) approved as an anabolic (bone-forming) osteoporosis medicine, and it has been studied in many randomized controlled trials and pooled in meta-analyses.
Source-linked reference figures with the population and study context alongside each amount. Study arms are not a starting dose, titration schedule, or personal treatment plan. Label records refer to the named approved medicine, not vendor products.
Hypoparathyroidism study (PMID 33538953). Titration schedule exactly as PMID 33538953 ↗ published it, step for step. pepmg does not compose or adjust schedules.
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FDA-approved label dose
20 mcg once daily
human · osteoporosis at high risk of fracture — postmenopausal women, men with primary or hypogonadal osteoporosis, and glucocorticoid-induced osteoporosis · FDA label (Forteo) · Route reported: subcutaneous
Dose administered in a randomised trial (Fracture Prevention Trial analysis) (human, postmenopausal women with osteoporosis, including mild or moderate renal impairment)
20 mcg/day or 40 mcg/day
human · postmenopausal women with osteoporosis, including mild or moderate renal impairment · randomised trial (Fracture Prevention Trial analysis) · Route reported: subcutaneous
Research use only — this reports what an FDA label or a peer-reviewed study published, tied to its species and study context. It is not medical advice, not a recommendation to use, and no dose here is generated by pepmg. Any dosing decision is for a qualified professional. Animal-study amounts do not establish a human dose.
All products listed are sold by third-party vendors for laboratory and research use only (RUO). Where an FDA label or a peer-reviewed study has published a dose, pepmg reports it with the source named, because that is safer than guessing. It is a report, not medical advice and not a recommendation to use anything. pepmg sells nothing and ships nothing. Listings are price-tracking data, not endorsements.
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