NDC 68180-590 – Ramipril

Ramipril 5 mg/1 · Capsule · Oral

Human Prescription Drug 3 recalls

Product NDC68180-590

Product details

Brand name
Ramipril
Generic name
Ramipril
Labeler
Lupin Pharmaceuticals, Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077626
Marketed since
June 10, 2008
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Ramipril →

Package NDC codes (4)

Package NDCDescriptionSince
68180-590-01100 CAPSULE in 1 BOTTLE (68180-590-01)Nov 20, 2024
68180-590-02500 CAPSULE in 1 BOTTLE (68180-590-02)Nov 25, 2024
68180-590-0990 CAPSULE in 1 BOTTLE (68180-590-09)Jun 10, 2008
68180-590-1090 CAPSULE in 1 BOTTLE (68180-590-10)Dec 10, 2024

Recalls mentioning this NDC

Other Ramipril products