Quick answers
- What is Ultra-Technekow V4?
- Ultra-Technekow V4 is a brand name of Technetium TC-99M, a prescription medicine. The FDA NDC Directory lists 13 Ultra-Technekow V4 products in 13 strengths and forms.
- Who makes Ultra-Technekow V4?
- Curium holds the FDA application for Ultra-Technekow V4 (NDA017243, approved November 23, 1973).
- Is there a generic or store brand of Ultra-Technekow V4?
- Other products of Technetium TC-99M are listed with the FDA, but none in exactly the same strength and form as a Ultra-Technekow V4 product.
- Has Ultra-Technekow V4 been recalled?
- No recall linked to Ultra-Technekow V4 products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Ultra-Technekow V4 is
Each Ultra-Technekow V4 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.
Technetium TC-99M · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| technetium TC-99M sodium pertechnetate 1 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 1.5 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 11 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 14 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 16 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 19 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 2 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 2.5 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 3 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 3.5 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 5 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 6 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
| technetium TC-99M sodium pertechnetate 7.5 Ci injection, solution (intravenous) | Ultra-Technekow V4 | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Technetium TC-99M →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA017243 | Curium | November 23, 1973 | 13 |
Companies that list Ultra-Technekow V4
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ultra-Technekow V4 products.
- Curium US LLC13 products
Recalls
No recall linked to Ultra-Technekow V4 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.