Lovastatin

Product NDC
0615-7690
11-digit product format
006157690
Labeler code
0615
Product ID
0615-7690_495dfca9-c3e6-4efe-a30a-e99906e735a2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Lovastatin
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA075828
Marketing category
ANDA
Marketing start
2001-12-17
Marketing end
0000-00-00
Substance
LOVASTATIN
Active strength
40 mg/1
Pharmacologic classes
HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0615-7690-392021-07-09C16284748780-19d75b9d0-a231-f424-e053-dadaa90a57cedb39f510-b247-46a4-a5ad-8da13697ec0c
0615-7690-392020-01-31C16284748780-19d75b9d0-a231-f424-e053-dadaa90a57cedb39f510-b247-46a4-a5ad-8da13697ec0c