Drugplain

ENOBY 60 mg/mL

Denosumab-qbde · INJECTION · Hikma Pharmaceuticals USA Inc.

No Recall History
Plain English

Enoby is a prescription injection used to treat osteoporosis and certain bone conditions by reducing bone loss. It works by blocking a protein that causes bone breakdown, helping to strengthen bones and reduce fracture risk.

Key Facts

Brand Name
ENOBY
Generic Name
Denosumab-qbde
NDC Code (Product)
0143-9165
Manufacturer
Hikma Pharmaceuticals USA Inc.
Strength
60 mg/mL
Dosage Form
INJECTION
Route
SUBCUTANEOUS
Marketing Status
Application #
BLA761439
Drug Class
RANK Ligand Inhibitor [EPC]
Marketing Start
01/08/2026

Recall History

No Recall History

Full Prescribing Information

Source: FDA Drug Label (SPL)For healthcare professionals

Indications & Usage

1 INDICATIONS AND USAGE Enoby is a RANK ligand (RANKL) inhibitor indicated for treatment: of postmenopausal women with osteoporosis at high risk for fracture ( 1.1 ) to increase bone mass in men with osteoporosis at high risk for fracture ( 1.2 ) of glucocorticoid-induced osteoporosis in men and women at high risk for fracture ( 1.3 ) to increase bone mass in men at high risk for fracture receiving androgen deprivation therapy for nonmetastatic prostate cancer ( 1.4 ) to increase bone mass in women at high risk for fracture receiving adjuvant aromatase inhibitor therapy for breast cancer ( 1.5 ) 1.1 Treatment of Postmenopausal Women with Osteoporosis at High Risk for Fracture Enoby is indicated for the treatment of postmenopausal women with osteoporosis at high risk for fracture, defined as a history of osteoporotic fracture, or multiple risk factors for fracture; or patients who have failed or are intolerant to other available osteoporosis therapy. In postmenopausal women with osteoporosis, denosumab reduces the incidence of vertebral, nonvertebral, and hip fractures [see Clinical Studies (14.1) ] . 1.2 Treatment to Increase Bone Mass in Men with Osteoporosis Enoby is indicated fo

Dosage & Administration

2 DOSAGE AND ADMINISTRATION Pregnancy must be ruled out prior to administration of Enoby. ( 2.1 ) Before initiating Enoby in patients with advanced chronic kidney disease, including dialysis patients, evaluate for the presence of chronic kidney disease mineral and bone disorder with intact parathyroid hormone, serum calcium, 25(OH) vitamin D, and 1,25(OH) 2 vitamin D. ( 2.2 , 5.1 , 8.6 ) Enoby should be administered by a healthcare provider. ( 2.3 ) Administer 60 mg every 6 months as a subcutaneous injection in the upper arm, upper thigh, or abdomen. ( 2.3 ) Instruct patients to take calcium 1000 mg daily and at least 400 IU vitamin D daily. ( 2.3 ) 2.1 Pregnancy Testing Prior to Initiation of Enoby Pregnancy must be ruled out prior to administration of Enoby. Perform pregnancy testing in all females of reproductive potential prior to administration of Enoby. Based on findings in animals, denosumab products can cause fetal harm when administered to pregnant women [see Use in Specific Populations (8.1 , 8.3) ] . 2.2 Laboratory Testing in Patients with Advanced Chronic Kidney Disease Prior to Initiation of Enoby In patients with advanced chronic kidney disease [i.e., estimated glomer

Contraindications

4 CONTRAINDICATIONS Enoby is contraindicated in: Patients with hypocalcemia: Pre-existing hypocalcemia must be corrected prior to initiating therapy with Enoby [see Warnings and Precautions (5.1) ] . Pregnant women: Denosumab products may cause fetal harm when administered to a pregnant woman. In women of reproductive potential, pregnancy testing should be performed prior to initiating treatment with Enoby [see Use in Specific Populations (8.1) ] . Patients with hypersensitivity to denosumab products: Enoby is contraindicated in patients with a history of systemic hypersensitivity to any component of the product. Reactions have included anaphylaxis, facial swelling, and urticaria [see Warnings and Precautions (5.3) , Adverse Reactions (6.2) ] . Hypocalcemia ( 4 , 5.1 ) Pregnancy ( 4 , 8.1 ) Known hypersensitivity to denosumab products ( 4 , 5.3 )

Adverse Reactions

6 ADVERSE REACTIONS The following serious adverse reactions are discussed below and also elsewhere in the labeling: Severe Hypocalcemia and Mineral Metabolism Changes [see Warnings and Precautions (5.1) ] Hypersensitivity [see Warnings and Precautions (5.3) ] Osteonecrosis of the Jaw [see Warnings and Precautions (5.4) ] Atypical Subtrochanteric and Diaphyseal Femoral Fractures [see Warnings and Precautions (5.5) ] Multiple Vertebral Fractures (MVF) Following Treatment Discontinuation [see Warnings and Precautions (5.6) ] Serious Infections [see Warnings and Precautions (5.7) ] Dermatologic Adverse Reactions [see Warnings and Precautions (5.8) ] The most common adverse reactions reported with denosumab products in patients with postmenopausal osteoporosis are back pain, pain in extremity, musculoskeletal pain, hypercholesterolemia, and cystitis. The most common adverse reactions reported with denosumab products in men with osteoporosis are back pain, arthralgia, and nasopharyngitis. The most common adverse reactions reported with denosumab products in patients with glucocorticoid-induced osteoporosis are back pain, hypertension, bronchitis, and headache. The most common (per patien

Frequently Asked Questions

What is ENOBY used for?

Enoby is a prescription injection used to treat osteoporosis and certain bone conditions by reducing bone loss. It works by blocking a protein that causes bone breakdown, helping to strengthen bones and reduce fracture risk.

Is ENOBY a controlled substance?

ENOBY is not classified as a controlled substance by the DEA.

What is the generic name for ENOBY?

The generic name for ENOBY is Denosumab-qbde. There are 1 other brand versions of Denosumab-qbde.

What is the NDC code for ENOBY 60 mg/mL?

The NDC (National Drug Code) for ENOBY 60 mg/mL is 0143-9165, listed by Hikma Pharmaceuticals USA Inc..

Product NDC

0143-9165

Package NDC

0143-9165-01

Other Denosumab-qbde Brands

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