Quick answers
- What is Methadose Dispersible?
- Methadose Dispersible is a brand name of Methadone hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Methadose Dispersible product in 1 strength and form.
- Who makes Methadose Dispersible?
- Specgx LLC holds the FDA application for Methadose Dispersible (ANDA074184, approved April 29, 1993).
- Is there a generic or store brand of Methadose Dispersible?
- Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a Methadose Dispersible product, 2 of them generic. Ask your pharmacist whether one is right for you.
- Has Methadose Dispersible been recalled?
- No recall linked to Methadose Dispersible products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Methadose Dispersible is
Each Methadose Dispersible 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 40 mg tablet (oral) | Methadose Dispersible | 3 products, 3 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
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA074184 | Specgx LLC | April 29, 1993 | 1 |
Companies that list Methadose Dispersible
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Methadose Dispersible products.
- SpecGx LLC1 product
Recalls
No recall linked to Methadose Dispersible 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.