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Brand-name prescription medicine

Procardia XL

Generic name: Nifedipine

FDA application holder: Pfizer

Strengths and generic versions

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

2Strengths and forms
28Same medicine, other names
1989FDA approval
0Recalls (FDA reports)

Quick answers

What is Procardia XL?
Procardia XL is a brand name of Nifedipine, a prescription medicine. The FDA NDC Directory lists 2 Procardia XL products in 2 strengths and forms.
Who makes Procardia XL?
Pfizer holds the FDA application for Procardia XL (NDA019684, approved September 6, 1989).
Is there a generic or store brand of Procardia XL?
Yes. The FDA NDC Directory lists 28 other products with the same active ingredients, strength and form as a Procardia XL product, 28 of them generic. Ask your pharmacist whether one is right for you.
Has Procardia XL been recalled?
No recall linked to Procardia XL products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Procardia XL is

Each Procardia XL 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.

Nifedipine · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
nifedipine 30 mg
tablet, film coated, extended release (oral)		 Procardia XL 14 products, 14 companies —
nifedipine 60 mg
tablet, film coated, extended release (oral)		 Procardia XL 14 products, 12 companies —

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Nifedipine →

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Procardia XL products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA019684PfizerSeptember 6, 19892

Companies that list Procardia XL

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

Recalls

No recall linked to Procardia XL 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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