Simvastatin

Product NDC
0615-7704
11-digit product format
006157704
Labeler code
0615
Product ID
0615-7704_169bb12d-2533-41f1-a1e0-891b1c5bcdf1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Simvastatin
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA077691
Marketing category
ANDA
Marketing start
2006-12-20
Marketing end
0000-00-00
Substance
SIMVASTATIN
Active strength
5 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
0615-7704-392021-08-31C16284748780-19d75b9d1-2061-f424-e053-dadaa90a57ce324a3791-d53e-4716-89cc-9516917407cf
0615-7704-392020-01-31C16284748780-19d75b9d1-2061-f424-e053-dadaa90a57ce324a3791-d53e-4716-89cc-9516917407cf