Quick answers
- What is Scandonest 3% Plain?
- Scandonest 3% Plain is a brand name of Mepivacaine hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Scandonest 3% Plain product in 1 strength and form.
- Who makes Scandonest 3% Plain?
- Deproco holds the FDA application for Scandonest 3% Plain (ANDA088387, approved October 10, 1984).
- Is there a generic or store brand of Scandonest 3% Plain?
- Yes. The FDA NDC Directory lists 10 other products with the same active ingredients, strength and form as a Scandonest 3% Plain product, 10 of them generic. Ask your pharmacist whether one is right for you.
- Has Scandonest 3% Plain been recalled?
- FDA enforcement reports list 1 recall of Scandonest 3% Plain products; the newest started November 20, 2020. A recall usually concerns specific lots, not every product.
What Scandonest 3% Plain is
Each Scandonest 3% Plain 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.
Mepivacaine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| mepivacaine hydrochloride 30 mg/mL injection, solution (subcutaneous) | Scandonest 3% Plain | 10 products, 9 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Mepivacaine hydrochloride →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA088387 | Deproco | October 10, 1984 | 1 |
Companies that list Scandonest 3% Plain
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Scandonest 3% Plain products.
- Septodont, Inc.1 product
Recalls
From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.
-
November 20, 2020 · Class III · Terminated · D-0127-2021
Labeling: Label mix-up
Scandonest 3% Plain (Mepivacaine Hydrochloride 3% without Vasoconstrictor), packaged in cartons of 50 cartridges (1.7 mL each), Rx only, Manufactured for SEPTODONT, Inc., Louisville, CO 80027, by Novocol Pharmaceutical o — Novocol Pharmaceutical of Canada, Inc.
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.