Quick answers
- What is Chloroprocaine Hci?
- Chloroprocaine Hci is a brand name of Chloroprocaine hydrochloride, a prescription medicine. The FDA NDC Directory lists 2 Chloroprocaine Hci products in 2 strengths and forms.
- Who makes Chloroprocaine Hci?
- Fresenius Kabi USA holds the FDA application for Chloroprocaine Hci (NDA009435, approved March 11, 1955).
- Is there a generic or store brand of Chloroprocaine Hci?
- Yes. The FDA NDC Directory lists 8 other products with the same active ingredients, strength and form as a Chloroprocaine Hci product, 4 of them generic. Ask your pharmacist whether one is right for you.
- Has Chloroprocaine Hci been recalled?
- No recall linked to Chloroprocaine Hci products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Chloroprocaine Hci is
Each Chloroprocaine Hci 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.
Chloroprocaine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| chloroprocaine hydrochloride 20 mg/mL injection, solution (epidural, infiltration, intracaudal, perineural) | Chloroprocaine Hci | 4 products, 3 companies | DailyMed |
| chloroprocaine hydrochloride 20 mg/mL injection, solution (infiltration, perineural) | Chloroprocaine Hci | 4 products, 3 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Chloroprocaine hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA009435 | Fresenius Kabi USA | March 11, 1955 | 2 |
Companies that list Chloroprocaine Hci
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Chloroprocaine Hci products.
- HF Acquisition Co LLC, DBA HealthFirst2 products
Recalls
No recall linked to Chloroprocaine Hci 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.