Quick answers
- What is Nimodipine used for?
- The FDA-approved label (Nymalize, Azurity Pharmaceuticals, Inc., August 30, 2024) says: “NYMALIZE is indicated for the improvement of neurological outcome by reducing the incidence and severity of ischemic deficits in adult patients with subarachnoid hemorrhage (SAH) from ruptured intracranial berry aneurysms regardless of their post-ictus neurological condition (i.e., Hunt and Hess Grades I-V). …” This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
- Does Nimodipine have a boxed warning?
- The label we quote has no boxed warning, but 2 of 4 FDA labels for this medicine do. Check the label of your own product.
- Is there a shortage of Nimodipine?
- No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
- Has Nimodipine been recalled?
- No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
- Who makes Nimodipine?
- 4 companies list prescription products of Nimodipine in the FDA NDC Directory, including Azurity Pharmaceuticals, Inc., Bionpharma Inc. and Camber Pharmaceuticals, Inc..
What Nimodipine is used for
Quoted from the “Indications and Usage” section of the FDA-approved label.
NYMALIZE is indicated for the improvement of neurological outcome by reducing the incidence and severity of ischemic deficits in adult patients with subarachnoid hemorrhage (SAH) from ruptured intracranial berry aneurysms regardless of their post-ictus neurological condition (i.e., Hunt and Hess Grades I-V). …
— FDA label: Nymalize, Azurity Pharmaceuticals, Inc., effective August 30, 2024. Read the full label on DailyMed →
The FDA has 4 labels for products of this medicine (different makers and forms); uses can differ between them. Check the label that comes with your own medicine.
This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.
Boxed warning
A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.
The label quoted above has no boxed warning.
2 of 4 FDA labels for this medicine have a boxed warning.
Forms and how it is given
| Dosage forms | Solution · Capsule, liquid filled |
|---|---|
| Route | Oral |
| Prescription products | 5 in the FDA NDC Directory |
| Brand names | Nymalize |
What pharmacies pay (NADAC)
The National Average Drug Acquisition Cost (NADAC) is the average price U.S. retail pharmacies paid to buy one unit of a medicine (one tablet, one mL or one gram), from a monthly survey of pharmacy invoices by the Centers for Medicare & Medicaid Services (CMS). State Medicaid programs use it to pay pharmacies.
This is not the price you pay. What you pay depends on your insurance (copay or coinsurance), your pharmacy and any discounts, and pharmacies also charge for filling a prescription. Ask your pharmacist or your health plan what your price will be.
| Strength and form | Generic or brand | Pharmacies pay |
|---|---|---|
| nimodipine 30 mg capsule, liquid filled | Generic | $1.46 per capsule |
NADAC list of November 4, 2026; these prices took effect on October 21, 2026. Shown only where a package’s NDC code matches the NADAC list exactly, and only for that exact strength and form: nothing is averaged across strengths. Strengths and forms not listed here have no NADAC price.
Source: NADAC (National Average Drug Acquisition Cost) 2026, data.medicaid.gov (CMS) →
Companies that list this medicine
Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.
- Azurity Pharmaceuticals, Inc.2 products
- Bionpharma Inc.1 product
- Camber Pharmaceuticals, Inc.1 product
- Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.1 product
FDA approval history
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Sponsor | Approved | Later changes approved |
|---|---|---|---|
| NDA203340 NYMALIZE | Azurity | May 10, 2013 | 7, latest August 28, 2024 2024: Manufacturing (CMC) · 2020: Manufacturing (CMC) · 2020: Manufacturing (CMC) |
Generic approvals (3)
- ANDA077811Heritage · May 2, 2007
- ANDA076740Bionpharma · January 17, 2008
- ANDA216937Annora Pharma · July 9, 2024
Shortage status
The FDA drug shortage list does not show these products.
Recalls
No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.
Official identifiers
| RxCUI (RxNorm) | 198037, 1423767, 2361311, 2361313 |
|---|---|
| SPL set ID of the quoted label | e660fa26-b5c4-4d6d-8887-9e22b6666a10 |
| FDA labels (SPL) | 4 |
| FDA applications | NDA203340, 3 ANDA |
| Active ingredients (FDA) | NIMODIPINE |
Sources
- FDA-approved label on DailyMed (National Library of Medicine) — Nymalize, Azurity Pharmaceuticals, Inc., effective August 30, 2024; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
- 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 recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →