Drugplain

Nimodipine 30 mg/1

Nimodipine · CAPSULE, LIQUID FILLED · BIONPHARMA INC.

No Recall History
Plain English

Nimodipine is a capsule, liquid filled containing nimodipine at 30 mg/1, taken oral. Manufactured by BIONPHARMA INC..

Key Facts

Brand Name
Nimodipine
Generic Name
Nimodipine
NDC Code (Product)
69452-209
Manufacturer
BIONPHARMA INC.
Strength
30 mg/1
Dosage Form
CAPSULE, LIQUID FILLED
Route
ORAL
Marketing Status
Application #
ANDA076740
Drug Class
Dihydropyridine Calcium Channel Blocker [EPC]
Marketing Start
11/21/2017

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective87 reports
off label use69 reports
hypotension57 reports
subarachnoid haemorrhage42 reports
dizziness32 reports
drug interaction32 reports
headache32 reports
renal failure31 reports
reversible cerebral vasoconstriction syndrome31 reports
condition aggravated28 reports

Frequently Asked Questions

What is Nimodipine used for?

Nimodipine contains Nimodipine. It is a capsule, liquid filled taken oral. Consult your doctor for specific uses.

Is Nimodipine a controlled substance?

Nimodipine is not classified as a controlled substance by the DEA.

What is the generic name for Nimodipine?

The generic name for Nimodipine is Nimodipine. There are 3 other brand versions of Nimodipine.

What is the NDC code for Nimodipine 30 mg/1?

The NDC (National Drug Code) for Nimodipine 30 mg/1 is 69452-209, listed by BIONPHARMA INC..

Product NDC

69452-209

Package NDC

69452-209-13

Other Nimodipine Dosages

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)