Hulio

Brand (proprietary) name

HULIO

Generic (nonproprietary) name

No authoritative public data was located for this field.

Active ingredient(s)

No authoritative public data was located for this field.

Strength(s)

No authoritative public data was located for this field.

Dosage form(s)

No authoritative public data was located for this field.

Route(s)

No authoritative public data was located for this field.

Manufacturer / labeler

Viatris Specialty LLCBiocon Biologics Inc.

Product class

Interchangeable biosimilar (derived from FDA marketing category and Purple Book license type)

Marketing category

BLA

Application number(s)

BLA761154

Earliest marketing start

Jul 1, 2023

Products / packages indexed

6 / 6

Also searchable as: HULIO · adalimumab-fkjp

Prescribing information on DailyMed (NLM)

• Q5140QQ-code: Temporary codesActiveDerived calculation

  Injection, adalimumab-fkjp, biosimilar, 1 mg

  Derived: 6 of 6 NDC package(s) for this drug appear in the CMS NDC–HCPCS crosswalk for Q5140. CMS quarters Q1 2025 – Q4 2025Not in the latest CMS crosswalk.

  Q-codes are temporary national codes recognized by Medicare. For drugs they include biosimilar products (Q51xx) and other drugs, biologicals, and skin substitutes that are not yet assigned a permanent code. Units follow the dosage in the descriptor.

No authoritative public data was located for this field.

Home infusion per diem (S-codes)

Medicare

Not payable by Medicare — CMS coverage code I (all 2 codes)

Part B pricing indicator

00 — Not separately priced by Part B (all 2 codes)

National payment amount

Which Medicare benefit pays for this drug?

• Coverage documents for Q5140 NCDs, LCDs, and Billing & Coding articles in the CMS Medicare Coverage Database that mention “Q5140”. Covered diagnosis codes are listed in the articles.
• Self-administered drug (SAD) exclusion lists Drugs each MAC excludes from “incident to” Part B coverage because they are usually self-administered.

No current Medicare Billing and Coding article lists Q5140.

• FDA NDC Directory data is submitted by labelers; FDA notes that inclusion does not mean the information was verified or that a product is approved, covered, or reimbursable.
• HCPCS links are derived from CMS NDC–HCPCS crosswalks, which support ASP-based Part B payment and are not a complete list of billable NDCs.
• Product class (brand, generic, biosimilar) is derived from the FDA marketing category and Purple Book license type, not from a commercial compendium.
• Payment limits are Medicare Part B national limits; they do not reflect payer contracts, OPPS rates, 340B pricing, or acquisition cost.
• Home infusion per diem S-codes are matched by therapy category from the FDA pharmacologic class and route, not from a CMS crosswalk. Payers choose which per diem codes they accept, and the right code can depend on the dosing schedule, infusion method, or daily volume.