Drugplain

Droxidopa 200 mg/1

Droxidopa · CAPSULE · Zydus Pharmaceuticals USA Inc.

No Recall History
Plain English

Droxidopa is a capsule containing droxidopa at 200 mg/1, taken oral. Manufactured by Zydus Pharmaceuticals USA Inc..

Key Facts

Brand Name
Droxidopa
Generic Name
Droxidopa
NDC Code (Product)
70710-1390
Manufacturer
Zydus Pharmaceuticals USA Inc.
Strength
200 mg/1
Dosage Form
CAPSULE
Route
ORAL
Marketing Status
Application #
ANDA211818
Marketing Start
02/19/2021

Recall History

No Recall History

Side Effects Reported to FDA

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

death218 reports
fall143 reports
dizziness90 reports
hallucination80 reports
hypotension66 reports
drug ineffective64 reports
loss of consciousness60 reports
hospitalisation56 reports
confusional state49 reports
blood pressure decreased45 reports

Frequently Asked Questions

What is Droxidopa used for?

Droxidopa contains Droxidopa. It is a capsule taken oral. Consult your doctor for specific uses.

Is Droxidopa a controlled substance?

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

What is the generic name for Droxidopa?

The generic name for Droxidopa is Droxidopa. There are 5 other brand versions of Droxidopa.

What is the NDC code for Droxidopa 200 mg/1?

The NDC (National Drug Code) for Droxidopa 200 mg/1 is 70710-1390, listed by Zydus Pharmaceuticals USA Inc..

Product NDC

70710-1390

Package NDC

70710-1390-9

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

Data from openFDA · Public domain (CC0 1.0)