Quick answers
- What is Pylarify?
- Pylarify is a brand name of Piflufolastat F-18, a prescription medicine. The FDA NDC Directory lists 1 Pylarify product in 1 strength and form.
- Who makes Pylarify?
- Progenics Pharms Inc holds the FDA application for Pylarify (NDA214793, approved May 26, 2021).
- Is there a generic or store brand of Pylarify?
- Other products of Piflufolastat F-18 are listed with the FDA, but none in exactly the same strength and form as a Pylarify product.
- Has Pylarify been recalled?
- No recall linked to Pylarify products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Pylarify is
Each Pylarify 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.
Piflufolastat F-18 · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| piflufolastat F-18 80 mCi/mL injection (intravenous) | Pylarify | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Piflufolastat F-18 →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA214793 | Progenics Pharms Inc | May 26, 2021 | 1 |
Companies that list Pylarify
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Pylarify products.
- Progenics Pharmaceuticals, Inc.1 product
Recalls
No recall linked to Pylarify 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.