Quick answers
- What is Anectine?
- Anectine is a brand name of Succinylcholine, a prescription medicine. The FDA NDC Directory lists 3 Anectine products in 1 strength and form.
- Who makes Anectine?
- Sandoz holds the FDA application for Anectine (NDA008453, approved August 20, 1952). 1 other company (repackagers or distributors) also list Anectine products.
- Is there a generic or store brand of Anectine?
- Yes. The FDA NDC Directory lists 26 other products with the same active ingredients, strength and form as a Anectine product, 25 of them generic. Ask your pharmacist whether one is right for you.
- Has Anectine been recalled?
- No recall linked to Anectine products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Anectine is
Each Anectine 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.
Succinylcholine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| succinylcholine chloride 20 mg/mL injection, solution (intramuscular, intravenous, parenteral) | Anectine | 26 products, 21 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Succinylcholine →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA008453 | Sandoz | August 20, 1952 | 3 |
Companies that list Anectine
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Anectine products.
- Sandoz Inc2 products
- Civica, Inc.1 product
Recalls
No recall linked to Anectine 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.