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1.7 ML denosumab-bnht 70 MG/ML Injection — RxCUI 2717542

RxNorm drug concept · Semantic clinical drug
RxCUI 2717542 Semantic clinical drug · SCD ● Current RxNorm concept 2 FDA products 2 package NDCs Snapshot Jul 14, 2026

What you’re looking at: the standardized identity of one medicine, as the U.S. drug-data system sees it. Below — every FDA-listed product, package code, price benchmark, and billing code that maps to it.

🗂️ Key Facts

RxCUI2717542
Official name1.7 ML denosumab-bnht 70 MG/ML Injection
Concept typeSemantic clinical drug (SCD)
RxNorm statusCurrent RxNorm concept
Also known asdenosumab-bnht 120 MG per 1.7 ML Injection; denosumab-bnht 120 MG in 1.7 ML Injection; denosumab-bnht 70 MG/ML per 1.7 ML Injection
FDA products mapped2
Package NDCs mapped2
RxNorm release07/06/2026
Snapshot dataJul 14, 2026

📖 Skip the Codes — Read It in Plain English.

Our pharmacist-built guide to Denosumab Injection: what it is, how it’s used, side effects, and interactions.

📗 Our plain-language guide HelloPharmacist
  • It treats osteoporosis in people at high risk for fracture, including postmenopausal women, men, and people on long-term steroids. It also helps build bone in men on prostate cance...
  • Usually once every 6 months, given under the skin by a healthcare provider. If you miss one, get it as soon as you can and your 6-month schedule restarts from then. Take your calci...
  • Back pain, limb pain, and muscle or joint aches are most common. Some people notice bladder infections, cold symptoms, or headaches. Call your doctor for muscle cramps or tingling,...
  • No dose change is needed, but advanced kidney disease or dialysis raises the risk of severe low calcium, which can be life-threatening. Your doctor should check your calcium and mi...
📖 Read our full Denosumab Injection guide →

🕸️ Concept Web — How 1.7 ML denosumab-bnht 70 MG/ML Injection Connects

One RxCUI never lives alone. Follow the path from the raw ingredient down to the exact strength-and-form concepts FDA products carry — every stop is a real RxNorm concept with its own identifier. Hover or focus any chip for what it means.
This page's concept 1.7 ML denosumab-bnht 70 MG/ML Injection RxCUI 2717542

Every web starts here: one RxCUI, one fixed meaning in the RxNorm vocabulary.

  1. Ingredients 2

    The active substance itself — no strength, form, or brand attached yet.

    • Denosumab 993449
    • Denosumab-bnht 2717527
  2. Brand names 1

    The same medicine's trade names. A brand name alone says nothing about strength or form.

    • Bomyntra 2717544
  3. Dose forms 9

    The ingredient poured into a form — tablet, solution, cream — still without one fixed strength.

    • Denosumab Injection 1655915
    • Denosumab-bnht Injection 2717541
    • Denosumab Injectable Product 1157742
    • Denosumab-bnht Injectable Product 2717529
    • Denosumab Injection [Bomyntra] 2717547
    • Denosumab-bnht Injection [Bomyntra] 2717548
    • Bomyntra Injectable Product 2717546
    • Injection 1649574
    • +1 more in this family
  4. Clinical & branded drugs 3

    Ingredient + strength + dose form. These are the concepts real FDA products actually carry.

Showing up to 8 concepts per family — 14 of 15 stored related concepts drawn.
These are official RxNorm vocabulary relationships — how concepts name and organize the same medicine. They do not establish therapeutic equivalence or substitutability: two concepts appearing in one web is never a statement that products can be swapped.

🔀 Generic ⇄ Brand Crosswalk

The same medicine has an unbranded (generic) identity and one or more brand-name identities — each with its own RxCUI. This is a naming relationship in RxNorm, not a statement that any two products are substitutable.

Generic (Clinical) Concepts

  • Denosumab-bnht 70 MG/ML SCDC · 2717540
  • Denosumab Injection SCDF · 1655915
  • Denosumab-bnht Injection SCDFP · 2717541
  • Denosumab Injectable Product SCDG · 1157742
  • Denosumab-bnht Injectable Product SCDGP · 2717529

Brand-Name Concepts

  • 1.7 ML denosumab-bnht 70 MG/ML Injection [Bomyntra] SBD · 2717549
  • Denosumab-bnht 70 MG/ML [Bomyntra] SBDC · 2717545
  • Denosumab Injection [Bomyntra] SBDF · 2717547
  • Denosumab-bnht Injection [Bomyntra] SBDFP · 2717548
  • Bomyntra Injectable Product SBDG · 2717546
  • Bomyntra BN · 2717544

📦 FDA Products & Package NDCs

2 products · 2 package NDCs
2 package NDCs map to RxCUI 2717542 in the current snapshot — up to 50 per page. Each linked NDC opens its full package page.
Package NDC Package Brand / generic name Labeler Marketing start
65219-0670-01 1 VIAL, SINGLE-DOSE in 1 CARTON (65219-670-01) / 1.7 mL in... BOMYNTRA Fresenius Kabi USA, LLC 2025-06-30
65219-0672-01 1 SYRINGE, PLASTIC in 1 CARTON (65219-672-01) / 1.7 mL in 1... BOMYNTRA Fresenius Kabi USA, LLC 2025-06-30
Observed labelers: Fresenius Kabi USA, LLC (2) — this is the FDA-listed mapping footprint, not sales, inventory, availability, or market share.

🧾 Billing Codes (HCPCS)

Medical billing codes (HCPCS "J-codes") that connect to this concept's packages — used mostly when a clinic or hospital bills for a drug it administers. Each code links to its full billing page.
CodeDescriptorMapped packagesSources
Q5158 Inj, denosumab-bnht, 1 mg 2 CMS
⚠ A crosswalk is not coverage: an NDC↔HCPCS mapping does not guarantee any payer covers or pays the code. Always verify the current payer policy before billing.

🗃️ Sources & Limits

Atlas generation902fddb9-e9c1-4004-bf4c-dba4d51037c7
openFDA export observedJul 14, 2026
RxNorm release07/06/2026
Methodology2026-07-full-catalog-v1
  • A shared RxCUI does not prove interchangeability. Products mapped to the same concept are not thereby equivalent or substitutable — equivalence is a separate, product-level determination.
  • Listing here does not establish approval or coverage. Appearing in this snapshot is a data observation, not an FDA approval status or a payer coverage decision.
  • Missing data never means zero. A silent dataset (no price, no billing code, no utilization) means no observation — not that the real-world value is zero.
  • Counts describe the mapping footprint. Product, package, and labeler counts are the FDA-listed mapping footprint in this snapshot — not sales, inventory, availability, or market share.
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product.

Machine-readable JSON

Reference information about drug-concept identifiers and public regulatory data — not medical advice. Talk to your pharmacist or prescriber about your own medication.