Quick answers
- What is Lignospan Forte?
- Lignospan Forte is a brand name of Lidocaine hydrochloride and epinephrine, a prescription medicine. The FDA NDC Directory lists 1 Lignospan Forte product in 1 strength and form.
- Who makes Lignospan Forte?
- Deproco holds the FDA application for Lignospan Forte (ANDA088389, approved September 30, 2009).
- Is there a generic or store brand of Lignospan Forte?
- Yes. The FDA NDC Directory lists 5 other products with the same active ingredients, strength and form as a Lignospan Forte product, 5 of them generic. Ask your pharmacist whether one is right for you.
- Has Lignospan Forte been recalled?
- No recall linked to Lignospan Forte products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Lignospan Forte is
Each Lignospan Forte 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.
Lidocaine hydrochloride and epinephrine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| epinephrine bitartrate 0.02 mg/mL · lidocaine hydrochloride 20 mg/mL injection, solution (submucosal) | Lignospan Forte | 5 products, 5 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Lidocaine hydrochloride and epinephrine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA088389 | Deproco | September 30, 2009 | 1 |
Companies that list Lignospan Forte
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Lignospan Forte products.
- Septodont, Inc.1 product
Recalls
No recall linked to Lignospan Forte 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.