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Brand-name prescription medicine

Provera

Generic name: Medroxyprogesterone acetate

FDA application holder: Pfizer

Strengths and generic versions Official label

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

At a glance

3Strengths and forms
26Same medicine, other names
1959FDA approval
0Recalls (FDA reports)

Quick answers

What is Provera?
Provera is a brand name of Medroxyprogesterone acetate, a prescription medicine. The FDA NDC Directory lists 3 Provera products in 3 strengths and forms.
Who makes Provera?
Pfizer holds the FDA application for Provera (NDA011839, approved June 18, 1959).
Is there a generic or store brand of Provera?
Yes. The FDA NDC Directory lists 26 other products with the same active ingredients, strength and form as a Provera product, 26 of them generic. Ask your pharmacist whether one is right for you.
Has Provera been recalled?
No recall linked to Provera products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Provera is

Each 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 formProduct namesSame medicine, other namesLabel
medroxyprogesterone acetate 10 mg
tablet (oral)		 Provera 13 products, 12 companies DailyMed
medroxyprogesterone acetate 2.5 mg
tablet (oral)		 Provera 7 products, 7 companies DailyMed
medroxyprogesterone acetate 5 mg
tablet (oral)		 Provera 6 products, 6 companies 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.
FDA applications of Provera products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA011839PfizerJune 18, 19593

Companies that list Provera

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Provera products.

Recalls

No recall linked to Provera products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. 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.

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