Quick answers
- What is Tencon?
- Tencon is a brand name of Butalbital and acetaminophen, a prescription medicine. The FDA NDC Directory lists 1 Tencon product in 1 strength and form.
- Who makes Tencon?
- Pharmobedient holds the FDA application for Tencon (ANDA089987, approved October 26, 1992).
- Is there a generic or store brand of Tencon?
- Yes. The FDA NDC Directory lists 5 other products with the same active ingredients, strength and form as a Tencon product, 5 of them generic. Ask your pharmacist whether one is right for you.
- Has Tencon been recalled?
- No recall linked to Tencon products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Tencon is
Each Tencon 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.
Butalbital and acetaminophen · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| acetaminophen 325 mg · butalbital 50 mg tablet (oral) | Tencon | 5 products, 5 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Butalbital and acetaminophen →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA089987 | Pharmobedient | October 26, 1992 | 1 |
Companies that list Tencon
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Tencon products.
- El Dorado Distributors LLC1 product
Recalls
No recall linked to Tencon 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.