Quick answers
- What is Ruby-Fill?
- Ruby-Fill is a brand name of Rubidium chloride RB-82, a prescription medicine. The FDA NDC Directory lists 1 Ruby-Fill product in 1 strength and form.
- Who makes Ruby-Fill?
- Jubilant holds the FDA application for Ruby-Fill (NDA202153, approved September 30, 2016).
- Is there a generic or store brand of Ruby-Fill?
- Other products of Rubidium chloride RB-82 are listed with the FDA, but none in exactly the same strength and form as a Ruby-Fill product.
- Has Ruby-Fill been recalled?
- No recall linked to Ruby-Fill products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Ruby-Fill is
Each Ruby-Fill 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.
Rubidium chloride RB-82 · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| rubidium chloride RB-82 100 mCi injection, solution (intravenous) | Ruby-Fill | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Rubidium chloride RB-82 →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA202153 | Jubilant | September 30, 2016 | 1 |
Companies that list Ruby-Fill
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Ruby-Fill products.
Recalls
No recall linked to Ruby-Fill 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.