NDC 60631-080 – Edarbi

Azilsartan Kamedoxomil 80 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC60631-080

Product details

Brand name
Edarbi
Generic name
Azilsartan kamedoxomil
Labeler
Azurity Pharmaceuticals, Inc.
Dosage form
Tablet
Route
Oral
Marketing category
NDA · NDA200796
Marketed since
February 1, 2013
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin 2 Receptor Blocker

Active ingredients

Uses, dosage, side effects and warnings for Edarbi →

Package NDC codes (2)

Package NDCDescriptionSince
60631-080-3030 TABLET in 1 BOTTLE (60631-080-30)Feb 1, 2013
60631-080-777 TABLET in 1 BOTTLE (60631-080-77)Feb 1, 2017

Recalls mentioning this NDC

Other Edarbi products