Quick answers
- What is Salagen?
- Salagen is a brand name of Pilocarpine hydrochloride, a prescription medicine. The FDA NDC Directory lists 2 Salagen products in 2 strengths and forms.
- Who makes Salagen?
- Advanz Pharma holds the FDA application for Salagen (NDA020237, approved March 22, 1994).
- Is there a generic or store brand of Salagen?
- Yes. The FDA NDC Directory lists 13 other products with the same active ingredients, strength and form as a Salagen product, 13 of them generic. Ask your pharmacist whether one is right for you.
- Has Salagen been recalled?
- No recall linked to Salagen products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Salagen is
Each Salagen 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.
Pilocarpine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| pilocarpine hydrochloride 5 mg tablet, film coated (oral) | Salagen | 10 products, 8 companies | DailyMed |
| pilocarpine hydrochloride 7.5 mg tablet, film coated (oral) | Salagen | 3 products, 3 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Pilocarpine hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA020237 | Advanz Pharma | March 22, 1994 | 2 |
Companies that list Salagen
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Salagen products.
- Advanz Pharma (US) Corp.2 products
Recalls
No recall linked to Salagen 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.