NDC 65862-041 – Lisinopril

Lisinopril 30 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC65862-041

Product details

Brand name
Lisinopril
Generic name
Lisinopril
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA077622
Marketed since
February 22, 2006
Listing expires
December 31, 2027
Pharmacologic class
Angiotensin Converting Enzyme Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Lisinopril →

Package NDC codes (5)

Package NDCDescriptionSince
65862-041-00100 TABLET in 1 BOTTLE (65862-041-00)Feb 22, 2006
65862-041-01100 TABLET in 1 BOTTLE (65862-041-01)Feb 22, 2006
65862-041-05500 TABLET in 1 BOTTLE (65862-041-05)Feb 22, 2006
65862-041-3030 TABLET in 1 BOTTLE (65862-041-30)Feb 22, 2006
65862-041-991000 TABLET in 1 BOTTLE (65862-041-99)Feb 22, 2006

Recalls mentioning this NDC

Other Lisinopril products