

A provider briefing on the Premarin shortage in 2026: supply timeline, prescribing implications, generic availability, and patient access tools.
Premarin (Conjugated Estrogens) remains one of the most widely prescribed hormone replacement therapies in the United States, with a patient population that spans menopausal symptom management, osteoporosis prevention, and hypoestrogenism treatment. In 2025 and into 2026, availability concerns have become a recurring topic in clinical settings.
This briefing provides prescribers with a current overview of Premarin supply status, the implications of the new generic entry, cost and access considerations, and practical tools to help patients maintain continuity of care.
The ASHP Drug Shortage Resource Center reported a shortage of Premarin Injection (Conjugated Estrogens for injection, 25 mg vials) beginning in May 2025. The shortage was attributed to manufacturing issues at Pfizer's production facility. The injection form is primarily used in acute care settings for the management of abnormal uterine bleeding due to hormonal imbalance.
By September 2025, Pfizer confirmed that Premarin Injection 25 mg vials were again available, and the ASHP listing was updated accordingly. No ongoing injection supply issues have been reported as of early 2026.
Ingenus Pharmaceuticals received FDA approval and immediately launched the first generic version of Premarin tablets — Conjugated Estrogens tablets, USP — in all five marketed strengths: 0.3 mg, 0.45 mg, 0.625 mg, 0.9 mg, and 1.25 mg. This landmark approval ended decades of Premarin's status as a brand-only product.
While neither Premarin tablets nor vaginal cream appear on the FDA's official drug shortage list, clinicians and patients continue to report intermittent difficulty finding specific formulations and strengths at retail pharmacies. These spot shortages are driven by distribution patterns rather than manufacturing deficiencies.
With the availability of generic Conjugated Estrogens tablets, pharmacists in most states will automatically substitute the generic unless the prescriber specifies "Dispense As Written" (DAW) or "Brand Medically Necessary." For the majority of patients, the generic is therapeutically equivalent (rated AB by the FDA) and clinically appropriate.
Providers should be aware that:
There is limited clinical rationale for requiring brand-name Premarin over the AB-rated generic in most patients. However, prescribers may consider brand specification for:
If neither brand Premarin nor generic Conjugated Estrogens is available, the following alternatives should be considered based on the patient's indication and risk profile:
For a patient-facing overview of these options, refer patients to alternatives to Premarin.
The key points for prescribers:
Cost remains a significant barrier for many Premarin patients:
Providers should proactively discuss cost with patients and direct them to savings resources. For a patient-friendly guide, refer them to how to save money on Premarin.
The Premarin market is in transition. The entry of generic competition in late 2025 should, over time, improve both availability and affordability. However, the initial adjustment period — with pharmacies and PBMs updating formularies and stocking decisions — may create temporary access friction through the first half of 2026.
Prescribers can support patients through this transition by:
For guidance on helping patients navigate pharmacy availability, see how to help your patients find Premarin in stock.
Premarin availability in 2026 is manageable but requires awareness. The injection shortage is resolved, a generic alternative now exists for tablets, and the overall supply chain is functional — but local spot shortages remain a reality for patients. Providers who stay informed and proactive can make a meaningful difference in their patients' continuity of care.
You focus on staying healthy. We'll handle the rest.
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