Quick answers
- What is TechneLite?
- TechneLite is a brand name of Technetium TC-99M, a prescription medicine. The FDA NDC Directory lists 4 TechneLite products in 1 strength and form.
- Who makes TechneLite?
- Shine holds the FDA application for TechneLite (NDA017771, approved November 16, 1976). 1 other company (repackagers or distributors) also list TechneLite products.
- Is there a generic or store brand of TechneLite?
- Other products of Technetium TC-99M are listed with the FDA, but none in exactly the same strength and form as a TechneLite product.
- Has TechneLite been recalled?
- No recall linked to TechneLite products (by their NDC code or label) appears in the FDA enforcement reports we use.
What TechneLite is
Each TechneLite 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 250 mCi/mL injection, solution (intravenous) | TechneLite | 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 |
|---|---|---|---|
| NDA017771 | Shine | November 16, 1976 | 4 |
Companies that list TechneLite
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of TechneLite products.
- Shine Spect USA, LLC2 products
- Lantheus Medical Imaging, Inc.2 products
Recalls
No recall linked to TechneLite 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.