Quick answers
- What is Migergot?
- Migergot is a brand name of Ergotamine tartrate and caffeine, a prescription medicine. The FDA NDC Directory lists 1 Migergot product in 1 strength and form.
- Who makes Migergot?
- Cosette holds the FDA application for Migergot (ANDA086557, approved October 4, 1983).
- Is there a generic or store brand of Migergot?
- Other products of Ergotamine tartrate and caffeine are listed with the FDA, but none in exactly the same strength and form as a Migergot product.
- Has Migergot been recalled?
- No recall linked to Migergot products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Migergot is
Each Migergot 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.
Ergotamine tartrate and caffeine · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| caffeine 100 mg · ergotamine tartrate 2 mg suppository (rectal) | Migergot | None listed | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Ergotamine tartrate and caffeine →
FDA approval
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA086557 | Cosette | October 4, 1983 | 1 |
Companies that list Migergot
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Migergot products.
- Cosette Pharmaceuticals, Inc.1 product
Recalls
No recall linked to Migergot 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.