Quick answers
- What is Pulmotech MAA?
- Pulmotech MAA is a brand name of Kit for the preparation of technetium tc 99M albumin aggregated, a prescription medicine. The FDA NDC Directory lists 1 Pulmotech MAA product in 1 strength and form.
- Who makes Pulmotech MAA?
- Cis Bio Intl holds the FDA application for Pulmotech MAA (BLA210089, approved March 20, 2020).
- Is there a generic or store brand of Pulmotech MAA?
- Other products of Kit for the preparation of technetium tc 99M albumin aggregated are listed with the FDA, but none in exactly the same strength and form as a Pulmotech MAA product.
- Has Pulmotech MAA been recalled?
- No recall linked to Pulmotech MAA products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Pulmotech MAA is
Each Pulmotech MAA 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.
Kit for the preparation of technetium tc 99M albumin aggregated · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| albumin aggregated 2 mg/15 mL injection, powder, lyophilized, for suspension (intraperitoneal, intravenous) | Pulmotech MAA | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Kit for the preparation of technetium tc 99M albumin aggregated →
FDA approval
- BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| BLA210089 | Cis Bio Intl | March 20, 2020 | 1 |
Companies that list Pulmotech MAA
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Pulmotech MAA products.
- Curium US LLC1 product
Recalls
No recall linked to Pulmotech MAA 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.