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Two medicines, side by side

Denosumab vs teriparatide

Denosumab and teriparatide are both labeled for osteoporosis. Drugs@FDA records approvals of denosumab since 2010 and of teriparatide since 2002. Pharmacies paid $1,862.74 per mL (Prolia 60 mg/mL syringe) and $479.95 per mL (Teriparatide 560 mcg/2.24 mL pen) (NADAC, October 7, 2026); the strengths differ and one is a brand and one a generic, so the two prices are not like for like. In FDA's classes, denosumab is a rank ligand inhibitor and teriparatide a parathyroid hormone analog.

Check it at the source: the denosumab FDA label on DailyMed (effective June 23, 2026); the teriparatide FDA label on DailyMed (effective August 3, 2026).

Highlights of the denosumab record

Denosumab (Prolia) · label of June 23, 2026

Used for

From the label: indications

Xgeva is a RANK ligand (RANKL) inhibitor indicated for: Prevention of skeletal-related events in patients with multiple myeloma and in patients with bone metastases from solid tumors. ( 1.1 ) Treatment of adults and skeletally mature adolescents with giant cell tumor of bone that is unresectable or where surgical resection is likely to result in severe morbidity. […]

On the market

Earliest approval on file
June 1, 2010
Generic labelers
none listed
Pharmacy cost
$1,862.74 per mL

Supply and safety

Shortage
No current entry
Recalls
2

Highlights of the teriparatide record

Teriparatide (Forteo) · label of August 3, 2026

Used for

From the label: indications

FORTEO is indicated: For the treatment of postmenopausal women with osteoporosis at high risk for fracture (defined herein as having a history of osteoporotic fracture or multiple risk factors for fracture) or who have failed or are intolerant to other available osteoporosis therapy. In postmenopausal women with osteoporosis, FORTEO reduces the risk of vertebral and nonvertebral fractures. […]

On the market

Earliest approval on file
November 26, 2002
Generic labelers
4 labelers
Pharmacy cost
$479.95 per mL

Supply and safety

Shortage
No current entry
Recalls
0

Source: FDA drug labels via openFDA (Denosumab label of June 23, 2026, Teriparatide label of August 3, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do denosumab and teriparatide differ on the record?

In FDA's classes, denosumab is a rank ligand inhibitor and teriparatide a parathyroid hormone analog.

How each works, in its label's words: Denosumab, “Xgeva binds to RANKL, a transmembrane or soluble protein essential for the formation, function, and survival of osteoclasts, the cells responsible for bone resorption, thereby modulating calcium …”; Teriparatide, “Endogenous 84-amino acid parathyroid hormone (PTH) is the primary regulator of calcium and phosphate metabolism in bone and kidney.”

Generics: denosumab none approved; teriparatide since 2023 (Drugs@FDA).

DenosumabTeriparatide
Labeled forOsteoporosisOsteoporosis
Pharmacologic classRANK Ligand InhibitorParathyroid Hormone Analog
How it works (label)Xgeva binds to RANKL, a transmembrane or soluble protein essential for the formation, function, and survival of osteoclasts, the cells responsible for bone resorption, thereby modulating calcium release from bone.Endogenous 84-amino acid parathyroid hormone (PTH) is the primary regulator of calcium and phosphate metabolism in bone and kidney.
Half-life (label)The mean elimination half-life was 28 days.n/a
Earliest approval on file (Drugs@FDA)June 1, 2010November 26, 2002
First generic approvednoneNovember 16, 2023
Generic labelers (NDC)none listed4 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$1,862.74 per mL (Prolia 60 mg/mL syringe)$479.95 per mL (Teriparatide 560 mcg/2.24 mL pen)
12-month price change+3%-43%
Boxed warningNoNo
Shortage nowNo current entryNo current entry
Recalls recorded20
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)201,378112,087
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What next?

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