

A provider-focused briefing on Prempro 0.3/1.5 28 Day availability in 2026, including supply timeline, prescribing implications, alternatives, and patient resources.
If your patients on Prempro 0.3/1.5 28 Day have been reporting difficulty filling their prescriptions, you're hearing a consistent signal from across the country. While this medication is not formally listed on the FDA drug shortage database as of early 2026, real-world availability has been inconsistent—particularly for the 0.3/1.5 mg strength.
This briefing covers the current supply landscape, prescribing considerations, therapeutic alternatives, and tools to help your patients maintain access to their hormone replacement therapy (HRT).
Prempro (conjugated estrogens/medroxyprogesterone acetate) is manufactured exclusively by Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer. The 0.3/1.5 mg formulation—the lowest available dose—has been subject to intermittent availability issues at the retail pharmacy level for several years.
Key supply factors:
Overall HRT prescribing volumes remain below their pre-WHI peak (2002), though there has been a gradual rebound as updated guidelines from the North American Menopause Society (NAMS) and the Endocrine Society have supported the use of HRT in appropriate candidates, particularly within the first 10 years of menopause onset.
For providers who have patients stabilized on Prempro 0.3/1.5, the availability challenges create several clinical considerations:
Abrupt discontinuation of combination HRT can lead to return of vasomotor symptoms, vaginal atrophy symptoms, and potential acceleration of bone loss in patients taking it for osteoporosis prevention. When patients cannot fill their Prempro prescription, continuity of therapy should be prioritized through one of the strategies outlined below.
If switching patients to an alternative HRT regimen, consider the following dose equivalence principles:
All combination estrogen-progestin therapies carry the same FDA boxed warning regarding increased risks of cardiovascular events (DVT, PE, stroke, MI), breast cancer, and probable dementia in women 65 and older. These warnings apply equally to Prempro and its alternatives. Prescribe at the lowest effective dose for the shortest duration consistent with treatment goals.
Based on pharmacy-level data and patient reports:
The Medfinder platform for providers offers real-time pharmacy stock data that can help you direct patients to pharmacies with confirmed availability in their area.
As a brand-name-only product, Prempro 0.3/1.5 carries significant cost implications for patients:
For patients facing cost barriers, generic alternatives like estradiol/norethindrone acetate (generic Activella) can reduce monthly costs to $30–$80. For a comprehensive overview, see our provider's guide to helping patients save money on Prempro.
Several resources can help you manage patients affected by Prempro 0.3/1.5 availability issues:
The supply outlook for Prempro 0.3/1.5 is unlikely to change dramatically in the near term. Without generic competition or additional manufacturers entering the market, availability will continue to depend on Pfizer's production and distribution decisions.
Providers should consider establishing a proactive plan for patients on Prempro 0.3/1.5:
While Prempro 0.3/1.5 28 Day remains a clinically valuable low-dose HRT option, its status as a brand-name-only product with inconsistent retail availability requires providers to be proactive. Having alternative regimens ready, understanding dose equivalencies, and leveraging tools like Medfinder for Providers can help ensure your patients maintain uninterrupted access to effective menopause management.
For patient-facing resources to share, see our guides on finding Prempro in stock and alternatives to Prempro.
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