Quick answers
- What is Nascobal?
- Nascobal is a brand name of Cyanocobalamin, a prescription medicine. The FDA NDC Directory lists 1 Nascobal product in 1 strength and form.
- Who makes Nascobal?
- Endo Operations holds the FDA application for Nascobal (NDA021642, approved January 31, 2005).
- Is there a generic or store brand of Nascobal?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a Nascobal product, 1 of them generic. Ask your pharmacist whether one is right for you.
- Has Nascobal been recalled?
- No recall linked to Nascobal products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Nascobal is
Each Nascobal 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.
Cyanocobalamin · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| cyanocobalamin 500 ug spray (nasal) | Nascobal | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Cyanocobalamin →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA021642 | Endo Operations | January 31, 2005 | 1 |
Companies that list Nascobal
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Nascobal products.
- Par Health USA, LLC1 product
Recalls
No recall linked to Nascobal 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.