Quick answers
- What is Testosterone enanthate used for?
- The FDA-approved label (Xyosted, Antares Pharma, Inc., July 1, 2025) says: “XYOSTED (testosterone enanthate) injection is an androgen indicated for testosterone replacement therapy in adult males for conditions associated with a deficiency or absence of endogenous testosterone. Primary hypogonadism (congenital or acquired) …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Testosterone enanthate have a boxed warning?
- No. None of the 3 FDA labels we found for this medicine has a boxed warning.
- Is there a shortage of Testosterone enanthate?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Testosterone enanthate been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Testosterone enanthate?
- 3 companies list prescription products of Testosterone enanthate in the FDA NDC Directory, including Antares Pharma, Inc., Hikma Pharmaceuticals USA Inc. and Eugia US LLC.
What Testosterone enanthate is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
XYOSTED (testosterone enanthate) injection is an androgen indicated for testosterone replacement therapy in adult males for conditions associated with a deficiency or absence of endogenous testosterone. Primary hypogonadism (congenital or acquired) …
— FDA label: Xyosted, Antares Pharma, Inc., effective July 1, 2025. Read the full label on DailyMed →
The FDA has 3 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
0 of 3 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Injection · Injection, solution |
|---|---|
| Route | Subcutaneous · Intramuscular |
| Prescription products | 5 in the FDA NDC Directory |
| Brand names | Xyosted |
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| testosterone enanthate 100 mg/0.5 mL injection | Brand: Xyosted | $316.44 per mL |
| testosterone enanthate 200 mg/mL injection, solution | Generic | $14.48 per mL |
| testosterone enanthate 50 mg/0.5 mL injection | Brand: Xyosted | $316.22 per mL |
| testosterone enanthate 75 mg/0.5 mL injection | Brand: Xyosted | $316.29 per mL |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Antares Pharma, Inc.3 products
- Hikma Pharmaceuticals USA Inc.1 product
- Eugia US LLC1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA209863 XYOSTED (AUTOINJECTOR) | Antares Pharma Inc | September 28, 2018 | 2, latest July 11, 2025 2025: Labeling · 2019: Labeling |
Generic approvals (2)
- ANDA091120Hikma Farmaceutica · September 18, 2012
- ANDA212659Eugia Pharma · February 28, 2024
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Xyosted, Antares Pharma, Inc., effective July 1, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →