Quick answers
- What is Idamycin PFS?
- Idamycin PFS is a brand name of Idarubicin hydrochloride, a prescription medicine. The FDA NDC Directory lists 3 Idamycin PFS products in 1 strength and form.
- Who makes Idamycin PFS?
- Pfizer holds the FDA application for Idamycin PFS (NDA050734, approved February 17, 1997).
- Is there a generic or store brand of Idamycin PFS?
- Other products of Idarubicin hydrochloride are listed with the FDA, but none in exactly the same strength and form as a Idamycin PFS product.
- Has Idamycin PFS been recalled?
- No recall linked to Idamycin PFS products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Idamycin PFS is
Each Idamycin PFS 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.
Idarubicin hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| idarubicin hydrochloride 1 mg/mL solution (intravenous) | Idamycin PFS | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Idarubicin hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA050734 | Pfizer | February 17, 1997 | 3 |
Companies that list Idamycin PFS
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Idamycin PFS products.
- Pfizer Laboratories Div Pfizer Inc3 products
Recalls
No recall linked to Idamycin PFS 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.