Drugplain

Ambrisentan 5 mg/1

Ambrisentan · TABLET, FILM COATED · Cipla USA Inc.

No Recall History
Plain English

Ambrisentan is a tablet, film coated containing ambrisentan at 5 mg/1, taken oral. Manufactured by Cipla USA Inc..

Key Facts

Brand Name
Ambrisentan
Generic Name
Ambrisentan
NDC Code (Product)
69097-386
Manufacturer
Cipla USA Inc.
Strength
5 mg/1
Dosage Form
TABLET, FILM COATED
Route
ORAL
Marketing Status
Application #
ANDA210715
Drug Class
Endothelin Receptor Antagonist [EPC]
Marketing Start
04/26/2019

Recall History

No Recall History

Side Effects Reported to FDA

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

dyspnoea9,117 reports
death7,173 reports
headache5,693 reports
pneumonia4,353 reports
diarrhoea4,013 reports
nausea3,375 reports
fatigue3,302 reports
dizziness3,065 reports
malaise2,625 reports
fluid retention2,468 reports

Full Prescribing Information

Full prescribing information not available for this product.

Frequently Asked Questions

What is Ambrisentan used for?

Ambrisentan contains Ambrisentan. It is a tablet, film coated taken oral. Consult your doctor for specific uses.

Is Ambrisentan a controlled substance?

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

What is the generic name for Ambrisentan?

The generic name for Ambrisentan is Ambrisentan. There are 4 other brand versions of Ambrisentan.

What is the NDC code for Ambrisentan 5 mg/1?

The NDC (National Drug Code) for Ambrisentan 5 mg/1 is 69097-386, listed by Cipla USA Inc..

Product NDC

69097-386

Package NDC

69097-386-02

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

Data from openFDA · Public domain (CC0 1.0)