Quick answers
- What is Prostin Vr Pediatric?
- Prostin Vr Pediatric is a brand name of Alprostadil, a prescription medicine. The FDA NDC Directory lists 2 Prostin Vr Pediatric products in 1 strength and form.
- Who makes Prostin Vr Pediatric?
- Pfizer holds the FDA application for Prostin Vr Pediatric (NDA018484, approved October 16, 1981).
- Is there a generic or store brand of Prostin Vr Pediatric?
- Other products of Alprostadil are listed with the FDA, but none in exactly the same strength and form as a Prostin Vr Pediatric product.
- Has Prostin Vr Pediatric been recalled?
- No recall linked to Prostin Vr Pediatric products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Prostin Vr Pediatric is
Each Prostin Vr Pediatric 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.
Alprostadil · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| alprostadil 500 ug/mL injection, solution (intravascular, intravenous) | Prostin Vr Pediatric | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Alprostadil →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA018484 | Pfizer | October 16, 1981 | 2 |
Companies that list Prostin Vr Pediatric
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Prostin Vr Pediatric products.
- Pharmacia & Upjohn Company LLC2 products
Recalls
No recall linked to Prostin Vr Pediatric 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.