Quick answers
- What is Depo-SubQ Provera?
- Depo-SubQ Provera is a brand name of Medroxyprogesterone acetate, a prescription medicine. The FDA NDC Directory lists 1 Depo-SubQ Provera product in 1 strength and form.
- Who makes Depo-SubQ Provera?
- Pfizer holds the FDA application for Depo-SubQ Provera (NDA021583, approved December 17, 2004).
- Is there a generic or store brand of Depo-SubQ Provera?
- Other products of Medroxyprogesterone acetate are listed with the FDA, but none in exactly the same strength and form as a Depo-SubQ Provera product.
- What do pharmacies pay for Depo-SubQ Provera?
- CMS lists a National Average Drug Acquisition Cost (NADAC) for 1 Depo-SubQ Provera strength and form (see the table below). That is what pharmacies pay to buy it, not what you pay: your price depends on your insurance and your pharmacy.
- Has Depo-SubQ Provera been recalled?
- No recall linked to Depo-SubQ Provera products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Depo-SubQ Provera is
Each Depo-SubQ Provera product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.
Medroxyprogesterone acetate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| medroxyprogesterone acetate 104 mg/0.65 mL injection, suspension (subcutaneous) | Depo-SubQ Provera | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Medroxyprogesterone acetate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021583 | Pfizer | December 17, 2004 | 1 |
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 |
|---|---|---|
| medroxyprogesterone acetate 104 mg/0.65 mL injection, suspension | Brand: Depo-SubQ Provera | $77.45 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 Depo-SubQ Provera
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Depo-SubQ Provera products.
- Pharmacia & Upjohn Company LLC1 product
Recalls
No recall linked to Depo-SubQ Provera products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- 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 labeling (SPL, 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
- NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026
Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.