Quick answers
- What is Soltamox?
- Soltamox is a brand name of Tamoxifen citrate, a prescription medicine. The FDA NDC Directory lists 1 Soltamox product in 1 strength and form.
- Who makes Soltamox?
- Mayne Pharma Commrcl holds the FDA application for Soltamox (NDA021807, approved October 29, 2005).
- Is there a generic or store brand of Soltamox?
- Other products of Tamoxifen citrate are listed with the FDA, but none in exactly the same strength and form as a Soltamox product.
- Has Soltamox been recalled?
- No recall linked to Soltamox products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Soltamox is
Each Soltamox 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.
Tamoxifen citrate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| tamoxifen citrate 20 mg/10 mL liquid (oral) | Soltamox | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Tamoxifen citrate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021807 | Mayne Pharma Commrcl | October 29, 2005 | 1 |
Companies that list Soltamox
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Soltamox products.
- Mayne Pharma1 product
Recalls
No recall linked to Soltamox 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.