Peptide

Teriparatide

FDA-approved product existsRecovery & tissue repair
Not yet scored

BioHarmony verdict

Awaiting review

No BioHarmony report yet. It is queued for review; until then, rely on the status and sources below.

What is Teriparatide?

FDA-approved teriparatide products exist for specified women and men with osteoporosis at high fracture risk and for glucocorticoid-associated osteoporosis in specified patients.

Dosing as published

Approved labelTeriparatide injection prescribing information for approved osteoporosis indications
PopulationWomen and men covered by the approved teriparatide indications
Dose20 mcg
RouteSubcutaneous injection into the thigh or abdomen
FrequencyOnce daily
DurationUse beyond 2 years during a lifetime is considered only when the patient remains at or returns to high fracture risk
PreparationReady-to-use 560 mcg/2.24 mL solution in a prefilled pen intended to deliver twenty-eight 20 mcg doses; no reconstitution. Discard the pen 28 days after first use.
Source: Dosage and Administration sections 2.1-2.3; Dosage Forms and Strengths section 3

More reported protocols

Members

Members can compare additional reported doses, schedules, and preparation notes.

Trust & sourcing

US approvalFDA-approved product exists
CompoundingFDA-approved products exist; compounded copies are not FDA approved
Last checked2026-07-13
Next review2026-10-11

Primary sources

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