NDC 0054-0109 – Ramipril

Ramipril 10 mg/1 · Capsule · Oral

Human Prescription Drug

Product NDC0054-0109

Product details

Brand name
Ramipril
Generic name
Ramipril
Labeler
Hikma Pharmaceuticals USA Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA077900
Marketed since
June 18, 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 (2)

Package NDCDescriptionSince
0054-0109-25100 CAPSULE in 1 BOTTLE (0054-0109-25)Jun 18, 2008
0054-0109-29500 CAPSULE in 1 BOTTLE (0054-0109-29)Jun 18, 2008

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