Bindinglaw

US · guidance

CMS Pub. 100-02, ch. 15, § 320.7.1

Determining Qualifying Home Infusion Drugs

activein force · 2026-08-25 – presentas-observed

In general, Medicare Part B covers a limited number of home infusion drugs through the

DME benefit if:

1. the drug is necessary for the effective use of an infusion pump classified as DME

and determined to be reasonable and necessary for administration of the drug; and

2. the drug being used with the pump is itself reasonable and necessary for the

treatment of an illness or injury.

Specifically, under this home infusion therapy services benefit, a home infusion drug

must require infusion through an external infusion pump that is covered under the DME

benefit. If the drug or biological can be infused through a disposable pump or by a

gravity drip, it does not meet this criterion.

Only certain types of infusion pumps are covered under the DME benefit. The Medicare

National Coverage Determinations Manual, Publication 100-03, Chapter 1, Section 280.1

describes the types of infusion pumps that are covered under the DME benefit. The DME

MACs then specify the details of which infusion drugs are covered with these pumps.

The drugs and biologicals identified in the DME Local Coverage Determination (LCD)

for External Infusion Pumps (L33794) qualify as home infusion drugs as long as they are

infused intravenously or subcutaneously over a period of 15 minutes or more, are not

classified as insulin for insulin pump use, and are not on a self-administered drug

exclusion list. These drugs continue to be paid for under the DME benefit as supply

drugs to the covered infusion pump. Any additional training and education services

needed for the patient to administer these drugs at home would be covered under this

home infusion therapy services benefit.

There are other infusion drugs covered under Part B that could potentially be added to the

DME LCD for External Infusion Pumps (L33794) and thus qualify for services under the

home infusion therapy services benefit. Allowing the DME MACs to maintain the list of

infusion drugs and biologicals ensures quarterly review of any and all medications that

meet the criteria for external infusion pumps, thus ensuring an up to date, inclusive

benefit.

History

(Rev. 10547, Issued: 12-31-20, Effective: 01-01-21, Implementation: 01-04-21)

Provenance

Source
cms.gov
Retrieved
2026-08-25
Edition
iom-2026-08-25
Content hash
06f5805af7539f76ded94142051db41d24af15bb4effd404dff26aff6b527e2a
View the official source →

The link goes to the issuing authority’s own document — the one we read to produce this record. Where a source publishes whole titles rather than sections, your browser may need a moment to jump to the provision.

Unofficial copy of government-published law, reproduced from official sources with full provenance. Not an official publication; verify against official sources before relying on it in a filing. Records in the 'guidance' corpus, and only that corpus, are sub-regulatory (interpretive guidelines, survey procedures) and are not binding law. Validity bounds follow each jurisdiction's declared temporalBasis.

Coverage · API docs

Bindinglaw

Point-in-time US law with the receipt attached. Source URL, retrieval time, content hash, and validity dates on every answer.

curl api.binding.law/v1/law/coverage

© 2026 binding.law · a Jubal, Inc. productAttorneys and firms never pay. Ever.