NDC 55111-229 – Pravastatin sodium

Pravastatin Sodium 10 mg/1 · Tablet · Oral

Human Prescription Drug 1 recall

Product NDC55111-229

Product details

Brand name
Pravastatin sodium
Generic name
Pravastatin sodium
Labeler
Dr.Reddy's Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076714
Marketed since
December 31, 2009
Listing expires
December 31, 2026
Pharmacologic class
HMG-CoA Reductase Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Pravastatin Sodium →

Package NDC codes (4)

Package NDCDescriptionSince
55111-229-01100 TABLET in 1 BOTTLE (55111-229-01)Dec 31, 2009
55111-229-05500 TABLET in 1 BOTTLE (55111-229-05)Dec 31, 2009
55111-229-3030 TABLET in 1 BOTTLE (55111-229-30)Dec 31, 2009
55111-229-9090 TABLET in 1 BOTTLE (55111-229-90)Dec 31, 2009

Recalls mentioning this NDC

Other Pravastatin Sodium products