Quick answers
- What is Septocaine and Epinephrine?
- Septocaine and Epinephrine is a brand name of Articaine hydrochloride and epinephrine, a prescription medicine. The FDA NDC Directory lists 2 Septocaine and Epinephrine products in 2 strengths and forms.
- Who makes Septocaine and Epinephrine?
- Deproco holds the FDA application for Septocaine and Epinephrine (NDA020971, approved April 3, 2000).
- Is there a generic or store brand of Septocaine and Epinephrine?
- Yes. The FDA NDC Directory lists 18 other products with the same active ingredients, strength and form as a Septocaine and Epinephrine product, 18 of them generic. Ask your pharmacist whether one is right for you.
- Has Septocaine and Epinephrine been recalled?
- No recall linked to Septocaine and Epinephrine products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Septocaine and Epinephrine is
Each Septocaine and Epinephrine 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.
Articaine hydrochloride and epinephrine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| articaine hydrochloride 40 mg/mL · epinephrine bitartrate 0.005 mg/mL injection, solution (submucosal) | Septocaine and Epinephrine | 8 products, 6 companies | DailyMed |
| articaine hydrochloride 40 mg/mL · epinephrine bitartrate 0.01 mg/mL injection, solution (submucosal) | Septocaine and Epinephrine | 10 products, 7 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Articaine hydrochloride and epinephrine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020971 | Deproco | April 3, 2000 | 2 |
Companies that list Septocaine and Epinephrine
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Septocaine and Epinephrine products.
- Septodont Inc.2 products
Recalls
No recall linked to Septocaine and Epinephrine products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Articaine hydrochloride and epinephrineThe medicine itself: side effects, interactions, dosage and generics
- Find a pharmacy near youAsk which price applies to you
- Latest FDA drug recallsNewest first
- All brand-name medicinesSearch by brand or product name
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.