Quick answers
- What is Marcaine Spinal?
- Marcaine Spinal is a brand name of Bupivacaine hydrochloride, a prescription medicine. The FDA NDC Directory lists 1 Marcaine Spinal product in 1 strength and form.
- Who makes Marcaine Spinal?
- Hospira holds the FDA application for Marcaine Spinal (NDA018692, approved May 4, 1984).
- Is there a generic or store brand of Marcaine Spinal?
- Yes. The FDA NDC Directory lists 15 other products with the same active ingredients, strength and form as a Marcaine Spinal product, 15 of them generic. Ask your pharmacist whether one is right for you.
- Has Marcaine Spinal been recalled?
- No recall linked to Marcaine Spinal products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Marcaine Spinal is
Each Marcaine Spinal 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.
Bupivacaine hydrochloride · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| bupivacaine hydrochloride 7.5 mg/mL injection, solution (subarachnoid) | Marcaine Spinal | 15 products, 9 companies | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Bupivacaine hydrochloride →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA018692 | Hospira | May 4, 1984 | 1 |
Companies that list Marcaine Spinal
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Marcaine Spinal products.
- Hospira, Inc.1 product
Recalls
No recall linked to Marcaine Spinal 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.