Quick answers
- What is Methadose Sugar-Free?
- Methadose Sugar-Free is a brand name of Methadone hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Methadose Sugar-Free product in 1 strength and form.
- Who makes Methadose Sugar-Free?
- Specgx LLC holds the FDA application for Methadose Sugar-Free (NDA017116, approved March 14, 1973).
- Is there a generic or store brand of Methadose Sugar-Free?
- Yes. The FDA NDC Directory lists 12 other products with the same active ingredients, strength and form as a Methadose Sugar-Free product, 11 of them generic. Ask your pharmacist whether one is right for you.
- Has Methadose Sugar-Free been recalled?
- No recall linked to Methadose Sugar-Free products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Methadose Sugar-Free is
Each Methadose Sugar-Free 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.
Methadone hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| methadone hydrochloride 10 mg/mL concentrate (oral) | Methadose Sugar-Free | 12 products, 7 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Methadone hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA017116 | Specgx LLC | March 14, 1973 | 1 |
Companies that list Methadose Sugar-Free
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Methadose Sugar-Free products.
- SpecGx LLC1 product
Recalls
No recall linked to Methadose Sugar-Free 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.