NDC 76282-673 – Ramipril

Ramipril 10 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC76282-673

Product details

Brand name
Ramipril
Generic name
Ramipril
Labeler
Exelan Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077900
Marketed since
June 18, 2008
Listing expires
December 31, 2026
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ramipril →

Package NDC codes (2)

Package NDCDescriptionSince
76282-673-01100 CAPSULE in 1 BOTTLE (76282-673-01)Jan 28, 2020
76282-673-05500 CAPSULE in 1 BOTTLE (76282-673-05)Oct 28, 2021

Recalls mentioning this NDC

Other Ramipril products