Quick answers
- What is Prezcobix Ped?
- Prezcobix Ped is a brand name of Darunavir ethanolate and cobicistat, a prescription medicine. The FDA NDC Directory lists 1 Prezcobix Ped product in 1 strength and form.
- Who makes Prezcobix Ped?
- Janssen Prods holds the FDA application for Prezcobix Ped (NDA220092, approved February 27, 2026).
- Is there a generic or store brand of Prezcobix Ped?
- Other products of Darunavir ethanolate and cobicistat are listed with the FDA, but none in exactly the same strength and form as a Prezcobix Ped product.
- Has Prezcobix Ped been recalled?
- No recall linked to Prezcobix Ped products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Prezcobix Ped is
Each Prezcobix Ped 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.
Darunavir ethanolate and cobicistat · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| cobicistat 90 mg · darunavir ethanolate 600 mg tablet, for suspension (oral) | Prezcobix Ped | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Darunavir ethanolate and cobicistat →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA220092 | Janssen Prods | February 27, 2026 | 1 |
Companies that list Prezcobix Ped
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Prezcobix Ped products.
- Janssen Products, LP1 product
Recalls
No recall linked to Prezcobix Ped 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.