Aetna modified CPB 0951 for brexanolone (Zulresso), effective February 14, 2026 — but the drug was pulled from the U.S. market in April 2025. Here's what billing teams need to know before a claim denial costs you.
Aetna updated its brexanolone coverage policy under CPB 0951 to reflect the market withdrawal of Zulresso. The policy governs HCPCS code J1632 (injection, brexanolone, 1 mg) and infusion administration codes 96365–96368. Any claim submitted for brexanolone billing after April 2025 is heading toward a wall — but the coverage criteria remain in the policy, which means your billing team needs to understand exactly where the lines are.
Quick-Reference Table
| Field | Detail |
|---|---|
| Payer | Aetna |
| Policy | Brexanolone (Zulresso) — CPB 0951 |
| Policy Code | CPB 0951 |
| Change Type | Modified |
| Effective Date | 2026-02-14 |
| Impact Level | Low (drug market withdrawal limits active billing exposure) |
| Specialties Affected | OB/GYN, psychiatry, maternal-fetal medicine, infusion centers |
| Key Action | Remove J1632 from active charge capture; document any pre-April 2025 claims against criteria before closing open encounters |
Aetna Brexanolone Coverage Criteria and Medical Necessity Requirements 2026
The real question for billing teams isn't whether Zulresso is still available. It isn't. The question is whether you have any open claims, prior authorizations, or encounters from before April 2025 that you still need to close correctly.
Aetna's coverage policy under CPB 0951 allows a one-time infusion of brexanolone for moderate to severe postpartum depression (PPD). The member must be 15 years of age or older. Three conditions must all be met at once.
First, the member must have a documented major depressive episode. That episode must have started no earlier than the third trimester of pregnancy and no later than four weeks following delivery. Aetna requires documentation using standardized rating scales — the Beck Depression Inventory (BDI), Hamilton Depression Rating Scale (HDRS), or Montgomery-Åsberg Depression Rating Scale (MADRS) all qualify.
Second, the member must be six months postpartum or less at the time of infusion.
Third — and this is the hard stop — Aetna covers only one infusion per pregnancy or childbirth. No repeat courses within the same pregnancy or childbirth event.
Prior authorization is required. This isn't optional language. Aetna requires precertification of brexanolone for all participating providers and members in applicable plan designs. Call (866) 752-7021 or fax (888) 267-3277 to initiate. Statement of Medical Necessity forms are available through Aetna's Specialty Pharmacy Precertification portal.
For any encounter billed before April 2025, medical necessity documentation needs to match these criteria exactly. A claim denial on an otherwise covered infusion — because the depression onset wasn't documented in the third trimester or the member was beyond six months postpartum — is avoidable. Check your records before you close those encounters.
This coverage policy applies to commercial medical plans. Medicare criteria follow a separate path. Check Aetna's Medicare Part B guidelines if you have Medicare Advantage exposure.
Aetna Brexanolone Exclusions and Non-Covered Indications
Aetna's position here is categorical: all indications other than moderate to severe PPD meeting the specific criteria above are experimental, investigational, or unproven. There are no gray areas in the policy language.
That means brexanolone for any other depressive disorder — major depressive disorder outside the postpartum window, bipolar depression, treatment-resistant depression — gets no coverage. Don't bill J1632 with a primary diagnosis outside F53.0 (postpartum depression) and expect reimbursement. You won't get it.
The ICD-10 code set in this policy is broad (more on that in the codes section below), but the clinical criteria are narrow. The wide diagnosis code range reflects what Aetna tracks for monitoring purposes, not an expansion of covered indications.
Coverage Indications at a Glance
| Indication | Status | Relevant Codes | Notes |
|---|---|---|---|
| Moderate to severe PPD, onset third trimester through 4 weeks postpartum, member ≤6 months postpartum, age ≥15 | Covered (one-time) | J1632, F53.0, 96365–96368 | Prior auth required; one infusion per pregnancy/childbirth only |
| PPD outside the defined onset or postpartum window | Not Covered | — | Fails medical necessity criteria |
| Any non-PPD depressive disorder | Not Covered / Experimental | — | All other indications deemed experimental, investigational, or unproven |
| Second or subsequent infusion (same pregnancy/childbirth) | Not Covered | — | Policy explicitly limits to one infusion per pregnancy/childbirth |
| Off-label use (any other neurological or psychiatric indication) | Not Covered / Experimental | — | No coverage outside approved PPD criteria |
Aetna Brexanolone Billing Guidelines and Action Items 2026
The drug is off the market. That doesn't mean your billing work is done. Here's what to do now.
| # | Action Item |
|---|---|
| 1 | Remove J1632 from active charge capture immediately. Zulresso was withdrawn from the U.S. market in April 2025. Any facility or practice that still has J1632 in an active charge master or superbill is creating unnecessary claim risk. Pull it now. |
| 2 | Audit open encounters from before April 2025. If your infusion center or OB/GYN practice administered brexanolone before the market withdrawal and those encounters aren't fully closed, work them before they age out. Check that documentation supports all three medical necessity criteria: standardized rating scale scores, onset timing, and six-month postpartum window. |
| 3 | Verify prior authorization status on any outstanding pre-April 2025 claims. Aetna requires precertification for brexanolone billing. If a prior auth was obtained but the claim wasn't fully adjudicated, confirm the auth number is on the claim and the service date falls within the auth window. |
| 4 | Pair J1632 with infusion administration codes 96365–96368 correctly. Codes 96365–96368 cover initial and additional infusion administration time. Make sure your infusion coding reflects actual documented infusion time from the clinical record. |
| 5 | Use F53.0 as the primary diagnosis code. This is the ICD-10-CM code for postpartum depression. It's the code that maps to the covered indication. Submitting J1632 with a primary diagnosis from the F31 (bipolar) or F41 (anxiety) ranges will generate a claim denial under this coverage policy. |
| 6 | Don't bill for repeat infusions within the same pregnancy or childbirth event. The policy allows one infusion per pregnancy or childbirth. The policy does not address scenarios involving separate future pregnancies — if that situation arises, talk to your compliance officer before billing. |
| 7 | If you have member or provider disputes on pre-2025 brexanolone claims, pull CPB 0951 as your reference. The effective date of February 14, 2026 reflects the most recent policy modification. For appeals on older dates of service, confirm which version of CPB 0951 Aetna was using at that time. PayerPolicy's version history tool shows you exactly what the criteria were on any date. |
If you're dealing with a complex prior authorization dispute or a denied claim from 2024 or early 2025, talk to your compliance officer before submitting an appeal. The criteria are specific enough that documentation gaps are the most common failure point.
| Previous Version | Current Version |
|---|---|
| Coverage is considered experimental and investigational for all indications | Coverage is considered medically necessary when specific criteria are met |
| Prior authorization is not required | Prior authorization is required for initial treatment |
| Documentation must include clinical history | Documentation must include clinical history |
| Re-review every 24 months | Re-review every 12 months with updated clinical documentation |
CPT, HCPCS, and ICD-10 Codes for Brexanolone Under CPB 0951
Covered HCPCS Codes (When Selection Criteria Are Met)
| Code | Type | Description |
|---|---|---|
| J1632 | HCPCS | Injection, brexanolone, 1 mg |
Key ICD-10-CM Diagnosis Codes
Aetna's CPB 0951 references a broad set of ICD-10-CM codes. The covered indication is F53.0. The remaining codes appear to reflect monitoring or exclusion tracking — they do not expand covered indications beyond PPD.
| Code | Description |
|---|---|
| F53.0 | Postpartum depression (primary covered indication) |
| F31.0 | Bipolar disorder |
| F31.1 | Bipolar disorder |
| F31.2 | Bipolar disorder |
| F31.3 | Bipolar disorder |
| F31.4 | Bipolar disorder |
| F31.5 | Bipolar disorder |
| F31.6 | Bipolar disorder |
| F31.7 | Bipolar disorder |
| F31.8 | Bipolar disorder |
| F31.9 | Bipolar disorder |
| F34.0–F39 | Mood disorders (range) |
| F41.0 | Other anxiety disorders |
| F41.1 | Other anxiety disorders |
| F41.2 | Other anxiety disorders |
| F41.3 | Other anxiety disorders |
| F41.4 | Other anxiety disorders |
| F41.5 | Other anxiety disorders |
| F41.6 | Other anxiety disorders |
| F41.7 | Other anxiety disorders |
| F41.8 | Other anxiety disorders |
| F41.9 | Other anxiety disorders |
| G10–G14 | Systemic atrophies primarily affecting the central nervous system |
| G20.A1–G26 | Extrapyramidal and movement disorders |
| G30.0–G32.89 | Other degenerative diseases of the nervous system |
| G35–G37.9 | Demyelinating diseases of the central nervous system |
| G40.001 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localization-related onset |
| G40.011 | Localization-related (focal) (partial) idiopathic epilepsy and epileptic syndromes with seizures of localization-related onset |
| G40.101 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures |
| G40.111 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with simple partial seizures |
| G40.201 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures |
| G40.211 | Localization-related (focal) (partial) symptomatic epilepsy and epileptic syndromes with complex partial seizures |
| G40.301 | Generalized idiopathic epilepsy and epileptic syndromes |
| G40.311 | Generalized idiopathic epilepsy and epileptic syndromes |
| G40.401 | Other generalized epilepsy and epileptic syndromes |
| G40.411 | Other generalized epilepsy and epileptic syndromes |
| G40.501 | Epileptic seizures related to external causes |
| G40.801 | Other epilepsy |
| G40.803 | Other epilepsy |
| G40.811 | Lennox-Gastaut syndrome |
| G40.813 | Lennox-Gastaut syndrome |
| G40.821 | Epileptic spasms |
| G40.823 | Epileptic spasms |
| G40.901 | Epilepsy, unspecified |
| G40.911 | Epilepsy, unspecified |
| G40.A01 | Absence epileptic syndrome |
| G40.A11 | Absence epileptic syndrome |
| G40.B01 | Juvenile myoclonic epilepsy |
| G40.B11 | Juvenile myoclonic epilepsy |
| G60.0–G65.2 | Polyneuropathies and other disorders of the peripheral nervous system |
| G70.00–G73.7 | Diseases of myoneural junction and muscle |
| G80.0–G80.9 | Cerebral palsy |
The neurological code ranges (G10–G80) in this policy are notable. They don't correspond to any covered indication for brexanolone. These likely appear in the policy's code set for tracking or exclusion documentation purposes. Don't let their presence suggest brexanolone has any covered application in epilepsy, movement disorders, or neurodegenerative conditions. It doesn't under this coverage policy.
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