Quick answers
- What is Chlorpromazine Hci?
- Chlorpromazine Hci is a brand name of Chlorpromazine hydrochloride, a prescription medicine. The FDA NDC Directory lists 3 Chlorpromazine Hci products in 1 strength and form.
- Who makes Chlorpromazine Hci?
- Dr Reddys holds the FDA application for Chlorpromazine Hci (ANDA080365, approved February 13, 1974). 1 other company (repackagers or distributors) also list Chlorpromazine Hci products.
- Is there a generic or store brand of Chlorpromazine Hci?
- Yes. The FDA NDC Directory lists 21 other products with the same active ingredients, strength and form as a Chlorpromazine Hci product, 21 of them generic. Ask your pharmacist whether one is right for you.
- Has Chlorpromazine Hci been recalled?
- No recall linked to Chlorpromazine Hci products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Chlorpromazine Hci is
Each Chlorpromazine 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.
Chlorpromazine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| chlorpromazine hydrochloride 25 mg/mL injection (intramuscular) | Chlorpromazine Hci | 21 products, 11 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Chlorpromazine hydrochloride →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA080365 | Dr Reddys | February 13, 1974 | 2 |
| ANDA083329 | Hikma | July 25, 1974 | 1 |
Companies that list Chlorpromazine Hci
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Chlorpromazine Hci products.
- Dr. Reddy's Laboratories Inc.2 products
- HF Acquisition Co LLC, DBA HealthFirst1 product
Recalls
No recall linked to Chlorpromazine 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.