Quick answers
- What is Lidocaine HCl and Epinephrine?
- Lidocaine HCl and Epinephrine is a brand name of Lidocaine hydrochloride,epinephrine bitartrate and Lidocaine hydrochloride and epinephrine, a prescription medicine. The FDA NDC Directory lists 3 Lidocaine HCl and Epinephrine products in 2 strengths and forms.
- Who makes Lidocaine HCl and Epinephrine?
- Fresenius Kabi USA holds the FDA application for Lidocaine HCl and Epinephrine (NDA006488, approved November 19, 1948).
- Is there a generic or store brand of Lidocaine HCl and Epinephrine?
- Yes. The FDA NDC Directory lists 9 other products with the same active ingredients, strength and form as a Lidocaine HCl and Epinephrine product, 6 of them generic. Ask your pharmacist whether one is right for you.
- Has Lidocaine HCl and Epinephrine been recalled?
- No recall linked to Lidocaine HCl and Epinephrine products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Lidocaine HCl and Epinephrine is
Each Lidocaine HCl 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.
Lidocaine hydrochloride,epinephrine bitartrate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| epinephrine bitartrate 0.01 mg/mL · lidocaine hydrochloride anhydrous 20 mg/mL injection, solution (infiltration, perineural) | Lidocaine Hci and Epinephrine | 3 products, 3 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Lidocaine hydrochloride,epinephrine bitartrate →
Lidocaine hydrochloride and epinephrine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| epinephrine 10 ug/mL · lidocaine hydrochloride 10 mg/mL injection, solution (infiltration, perineural) | Lidocaine Hci and Epinephrine | 6 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
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA006488 | Fresenius Kabi USA | November 19, 1948 | 2 |
| ANDA089644 | Hospira | June 21, 1988 | 1 |
Companies that list Lidocaine HCl and Epinephrine
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Lidocaine HCl and Epinephrine products.
- HF Acquisition Co LLC, DBA HealthFirst3 products
Recalls
No recall linked to Lidocaine HCl and Epinephrine products (by their NDC code or label) appears in the FDA enforcement reports.
Next steps
- Lidocaine hydrochloride,epinephrine bitartrateThe medicine itself: side effects, interactions, dosage and generics
- Lidocaine 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.