Quick answers
- What is Ziextenzo?
- Ziextenzo is a brand name of Pegfilgrastim-cbqv, a prescription medicine. The FDA NDC Directory lists 1 Ziextenzo product in 1 strength and form.
- Who makes Ziextenzo?
- Sandoz Inc holds the FDA application for Ziextenzo (BLA761045, approved November 4, 2019).
- Is there a generic or store brand of Ziextenzo?
- Yes. The FDA NDC Directory lists 4 other products with the same active ingredients, strength and form as a Ziextenzo product. Ask your pharmacist whether one is right for you.
- Has Ziextenzo been recalled?
- No recall linked to Ziextenzo products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Ziextenzo is
Each Ziextenzo 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.
Pegfilgrastim-cbqv · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| pegfilgrastim 6 mg/0.6 mL injection (subcutaneous) | Ziextenzo | 4 products, 4 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Pegfilgrastim-cbqv →
FDA approval
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| BLA761045 | Sandoz Inc | November 4, 2019 | 1 |
Companies that list Ziextenzo
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ziextenzo products.
- Sandoz Inc1 product
Recalls
No recall linked to Ziextenzo 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.