LOVASTATIN

Product NDC
54458-915
11-digit product format
544580915
Labeler code
54458
Product ID
54458-915_7e62b171-b224-4ffd-a785-f57ee81abeac
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
LOVASTATIN
Dosage form
TABLET
Route
ORAL
Labeler
International Laboratories, LLC
Application
ANDA075551
Marketing category
ANDA
Marketing start
2008-03-27
Marketing end
0000-00-00
Substance
LOVASTATIN
Active strength
20 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
54458-915-10EA - Each54458-9153f0ba688-e5f6-40d3-b299-484af95635d612012-07-24